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Items: 1 to 20 of 735

1.

rs1489858314 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    T>G [Show Flanks]
    Chromosome:
    11:13387129 (GRCh38)
    11:13408676 (GRCh37)
    Canonical SPDI:
    NC_000011.10:13387128:T:G
    Gene:
    ARNTL (Varview)
    Functional Consequence:
    non_coding_transcript_variant,3_prime_UTR_variant,genic_downstream_transcript_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    G=0./0 (ALFA)
    G=0.000004/1 (TOPMED)
    G=0.000007/1 (GnomAD)
    HGVS:
    NC_000011.10:g.13387129T>G, NC_000011.9:g.13408676T>G, NM_001178.6:c.*373T>G, NM_001178.5:c.*373T>G, NM_001178.4:c.*373T>G, XM_011520105.4:c.*373T>G, XM_011520105.3:c.*373T>G, XM_011520105.2:c.*373T>G, XM_011520105.1:c.*373T>G, XM_011520107.4:c.*373T>G, XM_011520107.3:c.*373T>G, XM_011520107.2:c.*373T>G, XM_011520107.1:c.*373T>G, XM_017017738.3:c.*373T>G, XM_017017738.2:c.*373T>G, XM_017017738.1:c.*373T>G, XM_017017739.3:c.*373T>G, XM_017017739.2:c.*373T>G, XM_017017739.1:c.*373T>G, NM_001030273.3:c.*373T>G, NM_001030273.2:c.*373T>G, NM_001030273.1:c.*373T>G, NM_001030272.3:c.*373T>G, NM_001030272.2:c.*373T>G, NM_001030272.1:c.*373T>G, NR_147789.2:n.2908T>G, NR_147789.1:n.2971T>G, NR_147787.2:n.2840T>G, NR_147787.1:n.2903T>G, NM_001351812.2:c.*373T>G, NM_001351812.1:c.*373T>G, NR_147790.2:n.2761T>G, NR_147790.1:n.2824T>G, NR_147791.2:n.2758T>G, NR_147791.1:n.2821T>G, NR_147788.2:n.2742T>G, NR_147788.1:n.2805T>G, NM_001351823.2:c.*373T>G, NM_001351823.1:c.*373T>G, NM_001351808.2:c.*373T>G, NM_001351808.1:c.*373T>G, NM_001351809.2:c.*373T>G, NM_001351809.1:c.*373T>G, NM_001351818.2:c.*373T>G, NM_001351818.1:c.*373T>G, NM_001351820.2:c.*373T>G, NM_001351820.1:c.*373T>G, NR_147785.2:n.2690T>G, NR_147785.1:n.2753T>G, NR_147786.2:n.2687T>G, NR_147786.1:n.2750T>G, NM_001351813.2:c.*373T>G, NM_001351813.1:c.*373T>G, NM_001351816.2:c.*373T>G, NM_001351816.1:c.*373T>G, NM_001351814.2:c.*373T>G, NM_001351814.1:c.*373T>G, NM_001297724.2:c.*373T>G, NM_001297724.1:c.*373T>G, NM_001297719.2:c.*373T>G, NM_001297719.1:c.*373T>G, NM_001351807.2:c.*373T>G, NM_001351807.1:c.*373T>G, NM_001351819.2:c.*373T>G, NM_001351819.1:c.*373T>G, NM_001351821.2:c.*373T>G, NM_001351821.1:c.*373T>G, NM_001297722.2:c.*373T>G, NM_001297722.1:c.*373T>G, NM_001351811.2:c.*373T>G, NM_001351811.1:c.*373T>G, NM_001351805.2:c.*373T>G, NM_001351805.1:c.*373T>G, NM_001351806.2:c.*373T>G, NM_001351806.1:c.*373T>G, NM_001351822.2:c.*373T>G, NM_001351822.1:c.*373T>G, XM_011520109.2:c.*373T>G, XM_011520109.1:c.*373T>G, XM_017017741.2:c.*373T>G, XM_017017741.1:c.*373T>G, NM_001351824.2:c.*373T>G, NM_001351824.1:c.*373T>G, NM_001351815.2:c.*373T>G, NM_001351815.1:c.*373T>G, NM_001351810.2:c.*373T>G, NM_001351810.1:c.*373T>G, NM_001351817.2:c.*373T>G, NM_001351817.1:c.*373T>G, XM_047426956.1:c.*373T>G, NM_001351804.1:c.*373T>G, XM_024448522.1:c.*373T>G, XM_047426953.1:c.*373T>G, XM_047426955.1:c.*373T>G, XM_047426952.1:c.*373T>G, XM_047426954.1:c.*373T>G

    2.

    rs1489586270 [Homo sapiens]
      Variant type:
      SNV
      Alleles:
      A>G [Show Flanks]
      Chromosome:
      11:13354384 (GRCh38)
      11:13375931 (GRCh37)
      Canonical SPDI:
      NC_000011.10:13354383:A:G
      Gene:
      ARNTL (Varview), LOC124902636 (Varview)
      Functional Consequence:
      coding_sequence_variant,500B_downstream_variant,non_coding_transcript_variant,genic_upstream_transcript_variant,downstream_transcript_variant,missense_variant,5_prime_UTR_variant,upstream_transcript_variant
      Validated:
      by frequency,by alfa,by cluster
      MAF:
      G=0./0 (ALFA)
      G=0.000004/1 (GnomAD_exomes)
      G=0.000008/2 (TOPMED)
      HGVS:
      NC_000011.10:g.13354384A>G, NC_000011.9:g.13375931A>G, NM_001178.6:c.76A>G, NM_001178.5:c.76A>G, NM_001178.4:c.76A>G, XM_011520105.4:c.205A>G, XM_011520105.3:c.205A>G, XM_011520105.2:c.205A>G, XM_011520105.1:c.76A>G, XM_011520107.4:c.205A>G, XM_011520107.3:c.205A>G, XM_011520107.2:c.205A>G, XM_011520107.1:c.76A>G, XM_017017738.3:c.205A>G, XM_017017738.2:c.205A>G, XM_017017738.1:c.205A>G, XM_017017739.3:c.205A>G, XM_017017739.2:c.205A>G, XM_017017739.1:c.205A>G, NM_001030273.3:c.-125A>G, NM_001030273.2:c.-125A>G, NM_001030273.1:c.-125A>G, NM_001030272.3:c.76A>G, NM_001030272.2:c.76A>G, NM_001030272.1:c.76A>G, NR_147789.2:n.417A>G, NR_147789.1:n.480A>G, NR_147787.2:n.417A>G, NR_147787.1:n.480A>G, NM_001351812.2:c.-100A>G, NM_001351812.1:c.-100A>G, NR_147790.2:n.417A>G, NR_147790.1:n.480A>G, NR_147791.2:n.417A>G, NR_147791.1:n.480A>G, NR_147788.2:n.472A>G, NR_147788.1:n.535A>G, NM_001351823.2:c.-125A>G, NM_001351823.1:c.-125A>G, NM_001351808.2:c.-125A>G, NM_001351808.1:c.-125A>G, NM_001351809.2:c.-100A>G, NM_001351809.1:c.-100A>G, NM_001351818.2:c.-125A>G, NM_001351818.1:c.-125A>G, NM_001351820.2:c.-118A>G, NM_001351820.1:c.-118A>G, NR_147785.2:n.417A>G, NR_147785.1:n.480A>G, NR_147786.2:n.417A>G, NR_147786.1:n.480A>G, NM_001351813.2:c.-125A>G, NM_001351813.1:c.-125A>G, NM_001351816.2:c.-125A>G, NM_001351816.1:c.-125A>G, NM_001351814.2:c.76A>G, NM_001351814.1:c.76A>G, NM_001297724.2:c.-118A>G, NM_001297724.1:c.-118A>G, NM_001297719.2:c.76A>G, NM_001297719.1:c.76A>G, NM_001351807.2:c.76A>G, NM_001351807.1:c.76A>G, NM_001351819.2:c.76A>G, NM_001351819.1:c.76A>G, NM_001351821.2:c.-125A>G, NM_001351821.1:c.-125A>G, NM_001297722.2:c.76A>G, NM_001297722.1:c.76A>G, NM_001351811.2:c.-667A>G, NM_001351811.1:c.-667A>G, NM_001351805.2:c.76A>G, NM_001351805.1:c.76A>G, NM_001351806.2:c.76A>G, NM_001351806.1:c.76A>G, NM_001351822.2:c.-125A>G, NM_001351822.1:c.-125A>G, XM_011520109.2:c.76A>G, XM_011520109.1:c.76A>G, XM_017017741.2:c.76A>G, XM_017017741.1:c.76A>G, NM_001351824.2:c.76A>G, NM_001351824.1:c.76A>G, NM_001351815.2:c.76A>G, NM_001351815.1:c.76A>G, NM_001351810.2:c.76A>G, NM_001351810.1:c.76A>G, NM_001351817.2:c.76A>G, NM_001351817.1:c.76A>G, XM_047426956.1:c.76A>G, NM_001351804.1:c.76A>G, XM_047426953.1:c.76A>G, XM_047426955.1:c.76A>G, XM_047426952.1:c.76A>G, XM_047426954.1:c.76A>G, XM_047426957.1:c.205A>G, XM_047426958.1:c.205A>G, NP_001169.3:p.Ser26Gly, XP_011518407.2:p.Ser69Gly, XP_011518409.2:p.Ser69Gly, XP_016873227.1:p.Ser69Gly, XP_016873228.1:p.Ser69Gly, NP_001025443.1:p.Ser26Gly, NP_001338743.1:p.Ser26Gly, NP_001284648.1:p.Ser26Gly, NP_001338736.1:p.Ser26Gly, NP_001338748.1:p.Ser26Gly, NP_001284651.1:p.Ser26Gly, NP_001338734.1:p.Ser26Gly, NP_001338735.1:p.Ser26Gly, XP_011518411.1:p.Ser26Gly, XP_016873230.1:p.Ser26Gly, NP_001338753.1:p.Ser26Gly, NP_001338744.1:p.Ser26Gly, NP_001338739.1:p.Ser26Gly, NP_001338746.1:p.Ser26Gly, XP_047282912.1:p.Ser26Gly, NP_001338733.1:p.Ser26Gly, XP_047282909.1:p.Ser26Gly, XP_047282911.1:p.Ser26Gly, XP_047282908.1:p.Ser26Gly, XP_047282910.1:p.Ser26Gly, XP_047282913.1:p.Ser69Gly, XP_047282914.1:p.Ser69Gly

      3.

      rs1488293367 [Homo sapiens]
        Variant type:
        SNV
        Alleles:
        C>T [Show Flanks]
        Chromosome:
        11:13386763 (GRCh38)
        11:13408310 (GRCh37)
        Canonical SPDI:
        NC_000011.10:13386762:C:T
        Gene:
        ARNTL (Varview)
        Functional Consequence:
        non_coding_transcript_variant,3_prime_UTR_variant,genic_downstream_transcript_variant
        Validated:
        by frequency
        MAF:
        T=0.000004/1 (GnomAD_exomes)
        HGVS:
        NC_000011.10:g.13386763C>T, NC_000011.9:g.13408310C>T, NM_001178.6:c.*7C>T, NM_001178.5:c.*7C>T, NM_001178.4:c.*7C>T, XM_011520105.4:c.*7C>T, XM_011520105.3:c.*7C>T, XM_011520105.2:c.*7C>T, XM_011520105.1:c.*7C>T, XM_011520107.4:c.*7C>T, XM_011520107.3:c.*7C>T, XM_011520107.2:c.*7C>T, XM_011520107.1:c.*7C>T, XM_017017738.3:c.*7C>T, XM_017017738.2:c.*7C>T, XM_017017738.1:c.*7C>T, XM_017017739.3:c.*7C>T, XM_017017739.2:c.*7C>T, XM_017017739.1:c.*7C>T, NM_001030273.3:c.*7C>T, NM_001030273.2:c.*7C>T, NM_001030273.1:c.*7C>T, NM_001030272.3:c.*7C>T, NM_001030272.2:c.*7C>T, NM_001030272.1:c.*7C>T, NR_147789.2:n.2542C>T, NR_147789.1:n.2605C>T, NR_147787.2:n.2474C>T, NR_147787.1:n.2537C>T, NM_001351812.2:c.*7C>T, NM_001351812.1:c.*7C>T, NR_147790.2:n.2395C>T, NR_147790.1:n.2458C>T, NR_147791.2:n.2392C>T, NR_147791.1:n.2455C>T, NR_147788.2:n.2376C>T, NR_147788.1:n.2439C>T, NM_001351823.2:c.*7C>T, NM_001351823.1:c.*7C>T, NM_001351808.2:c.*7C>T, NM_001351808.1:c.*7C>T, NM_001351809.2:c.*7C>T, NM_001351809.1:c.*7C>T, NM_001351818.2:c.*7C>T, NM_001351818.1:c.*7C>T, NM_001351820.2:c.*7C>T, NM_001351820.1:c.*7C>T, NR_147785.2:n.2324C>T, NR_147785.1:n.2387C>T, NR_147786.2:n.2321C>T, NR_147786.1:n.2384C>T, NM_001351813.2:c.*7C>T, NM_001351813.1:c.*7C>T, NM_001351816.2:c.*7C>T, NM_001351816.1:c.*7C>T, NM_001351814.2:c.*7C>T, NM_001351814.1:c.*7C>T, NM_001297724.2:c.*7C>T, NM_001297724.1:c.*7C>T, NM_001297719.2:c.*7C>T, NM_001297719.1:c.*7C>T, NM_001351807.2:c.*7C>T, NM_001351807.1:c.*7C>T, NM_001351819.2:c.*7C>T, NM_001351819.1:c.*7C>T, NM_001351821.2:c.*7C>T, NM_001351821.1:c.*7C>T, NM_001297722.2:c.*7C>T, NM_001297722.1:c.*7C>T, NM_001351811.2:c.*7C>T, NM_001351811.1:c.*7C>T, NM_001351805.2:c.*7C>T, NM_001351805.1:c.*7C>T, NM_001351806.2:c.*7C>T, NM_001351806.1:c.*7C>T, NM_001351822.2:c.*7C>T, NM_001351822.1:c.*7C>T, XM_011520109.2:c.*7C>T, XM_011520109.1:c.*7C>T, XM_017017741.2:c.*7C>T, XM_017017741.1:c.*7C>T, NM_001351824.2:c.*7C>T, NM_001351824.1:c.*7C>T, NM_001351815.2:c.*7C>T, NM_001351815.1:c.*7C>T, NM_001351810.2:c.*7C>T, NM_001351810.1:c.*7C>T, NM_001351817.2:c.*7C>T, NM_001351817.1:c.*7C>T, XM_047426956.1:c.*7C>T, NM_001351804.1:c.*7C>T, XM_024448522.1:c.*7C>T, XM_047426953.1:c.*7C>T, XM_047426955.1:c.*7C>T, XM_047426952.1:c.*7C>T, XM_047426954.1:c.*7C>T

        4.

        rs1487842422 [Homo sapiens]
          Variant type:
          SNV
          Alleles:
          T>C [Show Flanks]
          Chromosome:
          11:13387010 (GRCh38)
          11:13408557 (GRCh37)
          Canonical SPDI:
          NC_000011.10:13387009:T:C
          Gene:
          ARNTL (Varview)
          Functional Consequence:
          non_coding_transcript_variant,3_prime_UTR_variant,genic_downstream_transcript_variant
          Validated:
          by frequency,by alfa,by cluster
          MAF:
          C=0./0 (ALFA)
          C=0.000004/1 (TOPMED)
          C=0.000007/1 (GnomAD)
          HGVS:
          NC_000011.10:g.13387010T>C, NC_000011.9:g.13408557T>C, NM_001178.6:c.*254T>C, NM_001178.5:c.*254T>C, NM_001178.4:c.*254T>C, XM_011520105.4:c.*254T>C, XM_011520105.3:c.*254T>C, XM_011520105.2:c.*254T>C, XM_011520105.1:c.*254T>C, XM_011520107.4:c.*254T>C, XM_011520107.3:c.*254T>C, XM_011520107.2:c.*254T>C, XM_011520107.1:c.*254T>C, XM_017017738.3:c.*254T>C, XM_017017738.2:c.*254T>C, XM_017017738.1:c.*254T>C, XM_017017739.3:c.*254T>C, XM_017017739.2:c.*254T>C, XM_017017739.1:c.*254T>C, NM_001030273.3:c.*254T>C, NM_001030273.2:c.*254T>C, NM_001030273.1:c.*254T>C, NM_001030272.3:c.*254T>C, NM_001030272.2:c.*254T>C, NM_001030272.1:c.*254T>C, NR_147789.2:n.2789T>C, NR_147789.1:n.2852T>C, NR_147787.2:n.2721T>C, NR_147787.1:n.2784T>C, NM_001351812.2:c.*254T>C, NM_001351812.1:c.*254T>C, NR_147790.2:n.2642T>C, NR_147790.1:n.2705T>C, NR_147791.2:n.2639T>C, NR_147791.1:n.2702T>C, NR_147788.2:n.2623T>C, NR_147788.1:n.2686T>C, NM_001351823.2:c.*254T>C, NM_001351823.1:c.*254T>C, NM_001351808.2:c.*254T>C, NM_001351808.1:c.*254T>C, NM_001351809.2:c.*254T>C, NM_001351809.1:c.*254T>C, NM_001351818.2:c.*254T>C, NM_001351818.1:c.*254T>C, NM_001351820.2:c.*254T>C, NM_001351820.1:c.*254T>C, NR_147785.2:n.2571T>C, NR_147785.1:n.2634T>C, NR_147786.2:n.2568T>C, NR_147786.1:n.2631T>C, NM_001351813.2:c.*254T>C, NM_001351813.1:c.*254T>C, NM_001351816.2:c.*254T>C, NM_001351816.1:c.*254T>C, NM_001351814.2:c.*254T>C, NM_001351814.1:c.*254T>C, NM_001297724.2:c.*254T>C, NM_001297724.1:c.*254T>C, NM_001297719.2:c.*254T>C, NM_001297719.1:c.*254T>C, NM_001351807.2:c.*254T>C, NM_001351807.1:c.*254T>C, NM_001351819.2:c.*254T>C, NM_001351819.1:c.*254T>C, NM_001351821.2:c.*254T>C, NM_001351821.1:c.*254T>C, NM_001297722.2:c.*254T>C, NM_001297722.1:c.*254T>C, NM_001351811.2:c.*254T>C, NM_001351811.1:c.*254T>C, NM_001351805.2:c.*254T>C, NM_001351805.1:c.*254T>C, NM_001351806.2:c.*254T>C, NM_001351806.1:c.*254T>C, NM_001351822.2:c.*254T>C, NM_001351822.1:c.*254T>C, XM_011520109.2:c.*254T>C, XM_011520109.1:c.*254T>C, XM_017017741.2:c.*254T>C, XM_017017741.1:c.*254T>C, NM_001351824.2:c.*254T>C, NM_001351824.1:c.*254T>C, NM_001351815.2:c.*254T>C, NM_001351815.1:c.*254T>C, NM_001351810.2:c.*254T>C, NM_001351810.1:c.*254T>C, NM_001351817.2:c.*254T>C, NM_001351817.1:c.*254T>C, XM_047426956.1:c.*254T>C, NM_001351804.1:c.*254T>C, XM_024448522.1:c.*254T>C, XM_047426953.1:c.*254T>C, XM_047426955.1:c.*254T>C, XM_047426952.1:c.*254T>C, XM_047426954.1:c.*254T>C

          5.

          rs1487811736 [Homo sapiens]
            Variant type:
            SNV
            Alleles:
            C>A,T [Show Flanks]
            Chromosome:
            11:13387127 (GRCh38)
            11:13408674 (GRCh37)
            Canonical SPDI:
            NC_000011.10:13387126:C:A,NC_000011.10:13387126:C:T
            Gene:
            ARNTL (Varview)
            Functional Consequence:
            non_coding_transcript_variant,3_prime_UTR_variant,genic_downstream_transcript_variant
            Validated:
            by frequency,by alfa,by cluster
            MAF:
            T=0./0 (ALFA)
            A=0.000007/1 (GnomAD)
            HGVS:
            NC_000011.10:g.13387127C>A, NC_000011.10:g.13387127C>T, NC_000011.9:g.13408674C>A, NC_000011.9:g.13408674C>T, NM_001178.6:c.*371C>A, NM_001178.6:c.*371C>T, NM_001178.5:c.*371C>A, NM_001178.5:c.*371C>T, NM_001178.4:c.*371C>A, NM_001178.4:c.*371C>T, XM_011520105.4:c.*371C>A, XM_011520105.4:c.*371C>T, XM_011520105.3:c.*371C>A, XM_011520105.3:c.*371C>T, XM_011520105.2:c.*371C>A, XM_011520105.2:c.*371C>T, XM_011520105.1:c.*371C>A, XM_011520105.1:c.*371C>T, XM_011520107.4:c.*371C>A, XM_011520107.4:c.*371C>T, XM_011520107.3:c.*371C>A, XM_011520107.3:c.*371C>T, XM_011520107.2:c.*371C>A, XM_011520107.2:c.*371C>T, XM_011520107.1:c.*371C>A, XM_011520107.1:c.*371C>T, XM_017017738.3:c.*371C>A, XM_017017738.3:c.*371C>T, XM_017017738.2:c.*371C>A, XM_017017738.2:c.*371C>T, XM_017017738.1:c.*371C>A, XM_017017738.1:c.*371C>T, XM_017017739.3:c.*371C>A, XM_017017739.3:c.*371C>T, XM_017017739.2:c.*371C>A, XM_017017739.2:c.*371C>T, XM_017017739.1:c.*371C>A, XM_017017739.1:c.*371C>T, NM_001030273.3:c.*371C>A, NM_001030273.3:c.*371C>T, NM_001030273.2:c.*371C>A, NM_001030273.2:c.*371C>T, NM_001030273.1:c.*371C>A, NM_001030273.1:c.*371C>T, NM_001030272.3:c.*371C>A, NM_001030272.3:c.*371C>T, NM_001030272.2:c.*371C>A, NM_001030272.2:c.*371C>T, NM_001030272.1:c.*371C>A, NM_001030272.1:c.*371C>T, NR_147789.2:n.2906C>A, NR_147789.2:n.2906C>T, NR_147789.1:n.2969C>A, NR_147789.1:n.2969C>T, NR_147787.2:n.2838C>A, NR_147787.2:n.2838C>T, NR_147787.1:n.2901C>A, NR_147787.1:n.2901C>T, NM_001351812.2:c.*371C>A, NM_001351812.2:c.*371C>T, NM_001351812.1:c.*371C>A, NM_001351812.1:c.*371C>T, NR_147790.2:n.2759C>A, NR_147790.2:n.2759C>T, NR_147790.1:n.2822C>A, NR_147790.1:n.2822C>T, NR_147791.2:n.2756C>A, NR_147791.2:n.2756C>T, NR_147791.1:n.2819C>A, NR_147791.1:n.2819C>T, NR_147788.2:n.2740C>A, NR_147788.2:n.2740C>T, NR_147788.1:n.2803C>A, NR_147788.1:n.2803C>T, NM_001351823.2:c.*371C>A, NM_001351823.2:c.*371C>T, NM_001351823.1:c.*371C>A, NM_001351823.1:c.*371C>T, NM_001351808.2:c.*371C>A, NM_001351808.2:c.*371C>T, NM_001351808.1:c.*371C>A, NM_001351808.1:c.*371C>T, NM_001351809.2:c.*371C>A, NM_001351809.2:c.*371C>T, NM_001351809.1:c.*371C>A, NM_001351809.1:c.*371C>T, NM_001351818.2:c.*371C>A, NM_001351818.2:c.*371C>T, NM_001351818.1:c.*371C>A, NM_001351818.1:c.*371C>T, NM_001351820.2:c.*371C>A, NM_001351820.2:c.*371C>T, NM_001351820.1:c.*371C>A, NM_001351820.1:c.*371C>T, NR_147785.2:n.2688C>A, NR_147785.2:n.2688C>T, NR_147785.1:n.2751C>A, NR_147785.1:n.2751C>T, NR_147786.2:n.2685C>A, NR_147786.2:n.2685C>T, NR_147786.1:n.2748C>A, NR_147786.1:n.2748C>T, NM_001351813.2:c.*371C>A, NM_001351813.2:c.*371C>T, NM_001351813.1:c.*371C>A, NM_001351813.1:c.*371C>T, NM_001351816.2:c.*371C>A, NM_001351816.2:c.*371C>T, NM_001351816.1:c.*371C>A, NM_001351816.1:c.*371C>T, NM_001351814.2:c.*371C>A, NM_001351814.2:c.*371C>T, NM_001351814.1:c.*371C>A, NM_001351814.1:c.*371C>T, NM_001297724.2:c.*371C>A, NM_001297724.2:c.*371C>T, NM_001297724.1:c.*371C>A, NM_001297724.1:c.*371C>T, NM_001297719.2:c.*371C>A, NM_001297719.2:c.*371C>T, NM_001297719.1:c.*371C>A, NM_001297719.1:c.*371C>T, NM_001351807.2:c.*371C>A, NM_001351807.2:c.*371C>T, NM_001351807.1:c.*371C>A, NM_001351807.1:c.*371C>T, NM_001351819.2:c.*371C>A, NM_001351819.2:c.*371C>T, NM_001351819.1:c.*371C>A, NM_001351819.1:c.*371C>T, NM_001351821.2:c.*371C>A, NM_001351821.2:c.*371C>T, NM_001351821.1:c.*371C>A, NM_001351821.1:c.*371C>T, NM_001297722.2:c.*371C>A, NM_001297722.2:c.*371C>T, NM_001297722.1:c.*371C>A, NM_001297722.1:c.*371C>T, NM_001351811.2:c.*371C>A, NM_001351811.2:c.*371C>T, NM_001351811.1:c.*371C>A, NM_001351811.1:c.*371C>T, NM_001351805.2:c.*371C>A, NM_001351805.2:c.*371C>T, NM_001351805.1:c.*371C>A, NM_001351805.1:c.*371C>T, NM_001351806.2:c.*371C>A, NM_001351806.2:c.*371C>T, NM_001351806.1:c.*371C>A, NM_001351806.1:c.*371C>T, NM_001351822.2:c.*371C>A, NM_001351822.2:c.*371C>T, NM_001351822.1:c.*371C>A, NM_001351822.1:c.*371C>T, XM_011520109.2:c.*371C>A, XM_011520109.2:c.*371C>T, XM_011520109.1:c.*371C>A, XM_011520109.1:c.*371C>T, XM_017017741.2:c.*371C>A, XM_017017741.2:c.*371C>T, XM_017017741.1:c.*371C>A, XM_017017741.1:c.*371C>T, NM_001351824.2:c.*371C>A, NM_001351824.2:c.*371C>T, NM_001351824.1:c.*371C>A, NM_001351824.1:c.*371C>T, NM_001351815.2:c.*371C>A, NM_001351815.2:c.*371C>T, NM_001351815.1:c.*371C>A, NM_001351815.1:c.*371C>T, NM_001351810.2:c.*371C>A, NM_001351810.2:c.*371C>T, NM_001351810.1:c.*371C>A, NM_001351810.1:c.*371C>T, NM_001351817.2:c.*371C>A, NM_001351817.2:c.*371C>T, NM_001351817.1:c.*371C>A, NM_001351817.1:c.*371C>T, XM_047426956.1:c.*371C>A, XM_047426956.1:c.*371C>T, NM_001351804.1:c.*371C>A, NM_001351804.1:c.*371C>T, XM_024448522.1:c.*371C>A, XM_024448522.1:c.*371C>T, XM_047426953.1:c.*371C>A, XM_047426953.1:c.*371C>T, XM_047426955.1:c.*371C>A, XM_047426955.1:c.*371C>T, XM_047426952.1:c.*371C>A, XM_047426952.1:c.*371C>T, XM_047426954.1:c.*371C>A, XM_047426954.1:c.*371C>T

            6.

            rs1487477840 [Homo sapiens]
              Variant type:
              SNV
              Alleles:
              A>G [Show Flanks]
              Chromosome:
              11:13372339 (GRCh38)
              11:13393886 (GRCh37)
              Canonical SPDI:
              NC_000011.10:13372338:A:G
              Gene:
              ARNTL (Varview)
              Functional Consequence:
              coding_sequence_variant,genic_downstream_transcript_variant,non_coding_transcript_variant,intron_variant,missense_variant
              Validated:
              by frequency,by alfa,by cluster
              MAF:
              G=0./0 (ALFA)
              G=0.000007/1 (GnomAD)
              G=0.000015/4 (TOPMED)
              HGVS:
              NC_000011.10:g.13372339A>G, NC_000011.9:g.13393886A>G, NM_001178.6:c.994A>G, NM_001178.5:c.994A>G, NM_001178.4:c.994A>G, XM_011520105.4:c.1123A>G, XM_011520105.3:c.1123A>G, XM_011520105.2:c.1123A>G, XM_011520105.1:c.994A>G, XM_011520107.4:c.1123A>G, XM_011520107.3:c.1123A>G, XM_011520107.2:c.1123A>G, XM_011520107.1:c.994A>G, XM_017017738.3:c.1126A>G, XM_017017738.2:c.1126A>G, XM_017017738.1:c.1126A>G, XM_017017739.3:c.1126A>G, XM_017017739.2:c.1126A>G, XM_017017739.1:c.1126A>G, NM_001030273.3:c.865A>G, NM_001030273.2:c.865A>G, NM_001030273.1:c.865A>G, NM_001030272.3:c.994A>G, NM_001030272.2:c.994A>G, NM_001030272.1:c.994A>G, NR_147789.2:n.1406A>G, NR_147789.1:n.1469A>G, NR_147787.2:n.1338A>G, NR_147787.1:n.1401A>G, NM_001351812.2:c.946A>G, NM_001351812.1:c.946A>G, NR_147790.2:n.1409A>G, NR_147790.1:n.1472A>G, NR_147791.2:n.1406A>G, NR_147791.1:n.1469A>G, NR_147788.2:n.1390A>G, NR_147788.1:n.1453A>G, NM_001351823.2:c.868A>G, NM_001351823.1:c.868A>G, NM_001351808.2:c.868A>G, NM_001351808.1:c.868A>G, NM_001351809.2:c.946A>G, NM_001351809.1:c.946A>G, NM_001351818.2:c.865A>G, NM_001351818.1:c.865A>G, NM_001351820.2:c.868A>G, NM_001351820.1:c.868A>G, NR_147785.2:n.1338A>G, NR_147785.1:n.1401A>G, NR_147786.2:n.1335A>G, NR_147786.1:n.1398A>G, NM_001351813.2:c.865A>G, NM_001351813.1:c.865A>G, NM_001351816.2:c.868A>G, NM_001351816.1:c.868A>G, NM_001351814.2:c.997A>G, NM_001351814.1:c.997A>G, NM_001297724.2:c.868A>G, NM_001297724.1:c.868A>G, NM_001297719.2:c.997A>G, NM_001297719.1:c.997A>G, NM_001351807.2:c.997A>G, NM_001351807.1:c.997A>G, NM_001351819.2:c.994A>G, NM_001351819.1:c.994A>G, NM_001351821.2:c.868A>G, NM_001351821.1:c.868A>G, NM_001297722.2:c.997A>G, NM_001297722.1:c.997A>G, NM_001351811.2:c.247A>G, NM_001351811.1:c.247A>G, NM_001351805.2:c.958A>G, NM_001351805.1:c.958A>G, NM_001351806.2:c.955A>G, NM_001351806.1:c.955A>G, NM_001351822.2:c.868A>G, NM_001351822.1:c.868A>G, XM_011520109.2:c.997A>G, XM_011520109.1:c.997A>G, XM_017017741.2:c.994A>G, XM_017017741.1:c.994A>G, NM_001351824.2:c.997A>G, NM_001351824.1:c.997A>G, NM_001351815.2:c.994A>G, NM_001351815.1:c.994A>G, XM_047426956.1:c.997A>G, NM_001351804.1:c.994A>G, XM_024448522.1:c.946A>G, XM_047426953.1:c.997A>G, XM_047426955.1:c.997A>G, XM_047426952.1:c.997A>G, XM_047426954.1:c.997A>G, XM_047426957.1:c.1126A>G, NP_001169.3:p.Ile332Val, XP_011518407.2:p.Ile375Val, XP_011518409.2:p.Ile375Val, XP_016873227.1:p.Ile376Val, XP_016873228.1:p.Ile376Val, NP_001025444.1:p.Ile289Val, NP_001025443.1:p.Ile332Val, NP_001338741.1:p.Ile316Val, NP_001338752.1:p.Ile290Val, NP_001338737.1:p.Ile290Val, NP_001338738.1:p.Ile316Val, NP_001338747.1:p.Ile289Val, NP_001338749.1:p.Ile290Val, NP_001338742.1:p.Ile289Val, NP_001338745.1:p.Ile290Val, NP_001338743.1:p.Ile333Val, NP_001284653.1:p.Ile290Val, NP_001284648.1:p.Ile333Val, NP_001338736.1:p.Ile333Val, NP_001338748.1:p.Ile332Val, NP_001338750.1:p.Ile290Val, NP_001284651.1:p.Ile333Val, NP_001338740.1:p.Ile83Val, NP_001338734.1:p.Ile320Val, NP_001338735.1:p.Ile319Val, NP_001338751.1:p.Ile290Val, XP_011518411.1:p.Ile333Val, XP_016873230.1:p.Ile332Val, NP_001338753.1:p.Ile333Val, NP_001338744.1:p.Ile332Val, XP_047282912.1:p.Ile333Val, NP_001338733.1:p.Ile332Val, XP_024304290.1:p.Ile316Val, XP_047282909.1:p.Ile333Val, XP_047282911.1:p.Ile333Val, XP_047282908.1:p.Ile333Val, XP_047282910.1:p.Ile333Val, XP_047282913.1:p.Ile376Val

              7.

              rs1486537170 [Homo sapiens]
                Variant type:
                SNV
                Alleles:
                T>A [Show Flanks]
                Chromosome:
                11:13372316 (GRCh38)
                11:13393863 (GRCh37)
                Canonical SPDI:
                NC_000011.10:13372315:T:A
                Gene:
                ARNTL (Varview)
                Functional Consequence:
                coding_sequence_variant,genic_downstream_transcript_variant,non_coding_transcript_variant,intron_variant,missense_variant
                Validated:
                by frequency
                MAF:
                A=0.000004/1 (GnomAD_exomes)
                HGVS:
                NC_000011.10:g.13372316T>A, NC_000011.9:g.13393863T>A, NM_001178.6:c.971T>A, NM_001178.5:c.971T>A, NM_001178.4:c.971T>A, XM_011520105.4:c.1100T>A, XM_011520105.3:c.1100T>A, XM_011520105.2:c.1100T>A, XM_011520105.1:c.971T>A, XM_011520107.4:c.1100T>A, XM_011520107.3:c.1100T>A, XM_011520107.2:c.1100T>A, XM_011520107.1:c.971T>A, XM_017017738.3:c.1103T>A, XM_017017738.2:c.1103T>A, XM_017017738.1:c.1103T>A, XM_017017739.3:c.1103T>A, XM_017017739.2:c.1103T>A, XM_017017739.1:c.1103T>A, NM_001030273.3:c.842T>A, NM_001030273.2:c.842T>A, NM_001030273.1:c.842T>A, NM_001030272.3:c.971T>A, NM_001030272.2:c.971T>A, NM_001030272.1:c.971T>A, NR_147789.2:n.1383T>A, NR_147789.1:n.1446T>A, NR_147787.2:n.1315T>A, NR_147787.1:n.1378T>A, NM_001351812.2:c.923T>A, NM_001351812.1:c.923T>A, NR_147790.2:n.1386T>A, NR_147790.1:n.1449T>A, NR_147791.2:n.1383T>A, NR_147791.1:n.1446T>A, NR_147788.2:n.1367T>A, NR_147788.1:n.1430T>A, NM_001351823.2:c.845T>A, NM_001351823.1:c.845T>A, NM_001351808.2:c.845T>A, NM_001351808.1:c.845T>A, NM_001351809.2:c.923T>A, NM_001351809.1:c.923T>A, NM_001351818.2:c.842T>A, NM_001351818.1:c.842T>A, NM_001351820.2:c.845T>A, NM_001351820.1:c.845T>A, NR_147785.2:n.1315T>A, NR_147785.1:n.1378T>A, NR_147786.2:n.1312T>A, NR_147786.1:n.1375T>A, NM_001351813.2:c.842T>A, NM_001351813.1:c.842T>A, NM_001351816.2:c.845T>A, NM_001351816.1:c.845T>A, NM_001351814.2:c.974T>A, NM_001351814.1:c.974T>A, NM_001297724.2:c.845T>A, NM_001297724.1:c.845T>A, NM_001297719.2:c.974T>A, NM_001297719.1:c.974T>A, NM_001351807.2:c.974T>A, NM_001351807.1:c.974T>A, NM_001351819.2:c.971T>A, NM_001351819.1:c.971T>A, NM_001351821.2:c.845T>A, NM_001351821.1:c.845T>A, NM_001297722.2:c.974T>A, NM_001297722.1:c.974T>A, NM_001351811.2:c.224T>A, NM_001351811.1:c.224T>A, NM_001351805.2:c.935T>A, NM_001351805.1:c.935T>A, NM_001351806.2:c.932T>A, NM_001351806.1:c.932T>A, NM_001351822.2:c.845T>A, NM_001351822.1:c.845T>A, XM_011520109.2:c.974T>A, XM_011520109.1:c.974T>A, XM_017017741.2:c.971T>A, XM_017017741.1:c.971T>A, NM_001351824.2:c.974T>A, NM_001351824.1:c.974T>A, NM_001351815.2:c.971T>A, NM_001351815.1:c.971T>A, XM_047426956.1:c.974T>A, NM_001351804.1:c.971T>A, XM_024448522.1:c.923T>A, XM_047426953.1:c.974T>A, XM_047426955.1:c.974T>A, XM_047426952.1:c.974T>A, XM_047426954.1:c.974T>A, XM_047426957.1:c.1103T>A, NP_001169.3:p.Val324Asp, XP_011518407.2:p.Val367Asp, XP_011518409.2:p.Val367Asp, XP_016873227.1:p.Val368Asp, XP_016873228.1:p.Val368Asp, NP_001025444.1:p.Val281Asp, NP_001025443.1:p.Val324Asp, NP_001338741.1:p.Val308Asp, NP_001338752.1:p.Val282Asp, NP_001338737.1:p.Val282Asp, NP_001338738.1:p.Val308Asp, NP_001338747.1:p.Val281Asp, NP_001338749.1:p.Val282Asp, NP_001338742.1:p.Val281Asp, NP_001338745.1:p.Val282Asp, NP_001338743.1:p.Val325Asp, NP_001284653.1:p.Val282Asp, NP_001284648.1:p.Val325Asp, NP_001338736.1:p.Val325Asp, NP_001338748.1:p.Val324Asp, NP_001338750.1:p.Val282Asp, NP_001284651.1:p.Val325Asp, NP_001338740.1:p.Val75Asp, NP_001338734.1:p.Val312Asp, NP_001338735.1:p.Val311Asp, NP_001338751.1:p.Val282Asp, XP_011518411.1:p.Val325Asp, XP_016873230.1:p.Val324Asp, NP_001338753.1:p.Val325Asp, NP_001338744.1:p.Val324Asp, XP_047282912.1:p.Val325Asp, NP_001338733.1:p.Val324Asp, XP_024304290.1:p.Val308Asp, XP_047282909.1:p.Val325Asp, XP_047282911.1:p.Val325Asp, XP_047282908.1:p.Val325Asp, XP_047282910.1:p.Val325Asp, XP_047282913.1:p.Val368Asp

                8.

                rs1483665028 [Homo sapiens]
                  Variant type:
                  SNV
                  Alleles:
                  C>G [Show Flanks]
                  Chromosome:
                  11:13358518 (GRCh38)
                  11:13380065 (GRCh37)
                  Canonical SPDI:
                  NC_000011.10:13358517:C:G
                  Gene:
                  ARNTL (Varview), LOC124902636 (Varview)
                  Functional Consequence:
                  intron_variant,non_coding_transcript_variant,genic_upstream_transcript_variant,coding_sequence_variant,5_prime_UTR_variant,upstream_transcript_variant,missense_variant
                  Validated:
                  by frequency
                  MAF:
                  G=0.000004/1 (GnomAD_exomes)
                  HGVS:
                  NC_000011.10:g.13358518C>G, NC_000011.9:g.13380065C>G, NM_001178.6:c.306C>G, NM_001178.5:c.306C>G, NM_001178.4:c.306C>G, XM_011520105.4:c.435C>G, XM_011520105.3:c.435C>G, XM_011520105.2:c.435C>G, XM_011520105.1:c.306C>G, XM_011520107.4:c.435C>G, XM_011520107.3:c.435C>G, XM_011520107.2:c.435C>G, XM_011520107.1:c.306C>G, XM_017017738.3:c.435C>G, XM_017017738.2:c.435C>G, XM_017017738.1:c.435C>G, XM_017017739.3:c.435C>G, XM_017017739.2:c.435C>G, XM_017017739.1:c.435C>G, NM_001030273.3:c.177C>G, NM_001030273.2:c.177C>G, NM_001030273.1:c.177C>G, NM_001030272.3:c.306C>G, NM_001030272.2:c.306C>G, NM_001030272.1:c.306C>G, NR_147789.2:n.718C>G, NR_147789.1:n.781C>G, NR_147787.2:n.647C>G, NR_147787.1:n.710C>G, NM_001351812.2:c.255C>G, NM_001351812.1:c.255C>G, NR_147790.2:n.718C>G, NR_147790.1:n.781C>G, NR_147791.2:n.718C>G, NR_147791.1:n.781C>G, NR_147788.2:n.702C>G, NR_147788.1:n.765C>G, NM_001351823.2:c.177C>G, NM_001351823.1:c.177C>G, NM_001351808.2:c.177C>G, NM_001351808.1:c.177C>G, NM_001351809.2:c.255C>G, NM_001351809.1:c.255C>G, NM_001351818.2:c.177C>G, NM_001351818.1:c.177C>G, NM_001351820.2:c.177C>G, NM_001351820.1:c.177C>G, NR_147785.2:n.647C>G, NR_147785.1:n.710C>G, NR_147786.2:n.647C>G, NR_147786.1:n.710C>G, NM_001351813.2:c.177C>G, NM_001351813.1:c.177C>G, NM_001351816.2:c.177C>G, NM_001351816.1:c.177C>G, NM_001351814.2:c.306C>G, NM_001351814.1:c.306C>G, NM_001297724.2:c.177C>G, NM_001297724.1:c.177C>G, NM_001297719.2:c.306C>G, NM_001297719.1:c.306C>G, NM_001351807.2:c.306C>G, NM_001351807.1:c.306C>G, NM_001351819.2:c.306C>G, NM_001351819.1:c.306C>G, NM_001351821.2:c.177C>G, NM_001351821.1:c.177C>G, NM_001297722.2:c.306C>G, NM_001297722.1:c.306C>G, NM_001351811.2:c.-366C>G, NM_001351811.1:c.-366C>G, NM_001351805.2:c.267C>G, NM_001351805.1:c.267C>G, NM_001351806.2:c.267C>G, NM_001351806.1:c.267C>G, NM_001351822.2:c.177C>G, NM_001351822.1:c.177C>G, XM_011520109.2:c.306C>G, XM_011520109.1:c.306C>G, XM_017017741.2:c.306C>G, XM_017017741.1:c.306C>G, NM_001351824.2:c.306C>G, NM_001351824.1:c.306C>G, NM_001351815.2:c.306C>G, NM_001351815.1:c.306C>G, NM_001351810.2:c.306C>G, NM_001351810.1:c.306C>G, NM_001351817.2:c.306C>G, NM_001351817.1:c.306C>G, XM_047426956.1:c.306C>G, NM_001351804.1:c.306C>G, XM_024448522.1:c.255C>G, XM_047426953.1:c.306C>G, XM_047426955.1:c.306C>G, XM_047426952.1:c.306C>G, XM_047426954.1:c.306C>G, XM_047426957.1:c.435C>G, XM_047426958.1:c.435C>G, NP_001169.3:p.Cys102Trp, XP_011518407.2:p.Cys145Trp, XP_011518409.2:p.Cys145Trp, XP_016873227.1:p.Cys145Trp, XP_016873228.1:p.Cys145Trp, NP_001025444.1:p.Cys59Trp, NP_001025443.1:p.Cys102Trp, NP_001338741.1:p.Cys85Trp, NP_001338752.1:p.Cys59Trp, NP_001338737.1:p.Cys59Trp, NP_001338738.1:p.Cys85Trp, NP_001338747.1:p.Cys59Trp, NP_001338749.1:p.Cys59Trp, NP_001338742.1:p.Cys59Trp, NP_001338745.1:p.Cys59Trp, NP_001338743.1:p.Cys102Trp, NP_001284653.1:p.Cys59Trp, NP_001284648.1:p.Cys102Trp, NP_001338736.1:p.Cys102Trp, NP_001338748.1:p.Cys102Trp, NP_001338750.1:p.Cys59Trp, NP_001284651.1:p.Cys102Trp, NP_001338734.1:p.Cys89Trp, NP_001338735.1:p.Cys89Trp, NP_001338751.1:p.Cys59Trp, XP_011518411.1:p.Cys102Trp, XP_016873230.1:p.Cys102Trp, NP_001338753.1:p.Cys102Trp, NP_001338744.1:p.Cys102Trp, NP_001338739.1:p.Cys102Trp, NP_001338746.1:p.Cys102Trp, XP_047282912.1:p.Cys102Trp, NP_001338733.1:p.Cys102Trp, XP_024304290.1:p.Cys85Trp, XP_047282909.1:p.Cys102Trp, XP_047282911.1:p.Cys102Trp, XP_047282908.1:p.Cys102Trp, XP_047282910.1:p.Cys102Trp, XP_047282913.1:p.Cys145Trp, XP_047282914.1:p.Cys145Trp

                  9.

                  rs1483326003 [Homo sapiens]
                    Variant type:
                    SNV
                    Alleles:
                    A>C,G [Show Flanks]
                    Chromosome:
                    11:13276895 (GRCh38)
                    11:13298442 (GRCh37)
                    Canonical SPDI:
                    NC_000011.10:13276894:A:C,NC_000011.10:13276894:A:G
                    Gene:
                    ARNTL (Varview)
                    Functional Consequence:
                    5_prime_UTR_variant,upstream_transcript_variant,genic_upstream_transcript_variant
                    Validated:
                    by frequency,by alfa,by cluster
                    MAF:
                    G=0./0 (ALFA)
                    C=0.000007/1 (GnomAD)
                    HGVS:
                    NC_000011.10:g.13276895A>C, NC_000011.10:g.13276895A>G, NC_000011.9:g.13298442A>C, NC_000011.9:g.13298442A>G, XM_011520105.4:c.-130A>C, XM_011520105.4:c.-130A>G, XM_011520105.3:c.-130A>C, XM_011520105.3:c.-130A>G, XM_011520105.2:c.-130A>C, XM_011520105.2:c.-130A>G, XM_011520107.4:c.-130A>C, XM_011520107.4:c.-130A>G, XM_011520107.3:c.-130A>C, XM_011520107.3:c.-130A>G, XM_011520107.2:c.-130A>C, XM_011520107.2:c.-130A>G, XM_017017738.3:c.-130A>C, XM_017017738.3:c.-130A>G, XM_017017738.2:c.-130A>C, XM_017017738.2:c.-130A>G, XM_017017738.1:c.-130A>C, XM_017017738.1:c.-130A>G, XM_017017739.3:c.-130A>C, XM_017017739.3:c.-130A>G, XM_017017739.2:c.-130A>C, XM_017017739.2:c.-130A>G, XM_017017739.1:c.-130A>C, XM_017017739.1:c.-130A>G, NM_001351804.1:c.-440A>C, NM_001351804.1:c.-440A>G, XM_047426957.1:c.-130A>C, XM_047426957.1:c.-130A>G, XM_047426958.1:c.-130A>C, XM_047426958.1:c.-130A>G

                    10.

                    rs1482821657 [Homo sapiens]
                      Variant type:
                      SNV
                      Alleles:
                      G>A [Show Flanks]
                      Chromosome:
                      11:13387063 (GRCh38)
                      11:13408610 (GRCh37)
                      Canonical SPDI:
                      NC_000011.10:13387062:G:A
                      Gene:
                      ARNTL (Varview)
                      Functional Consequence:
                      3_prime_UTR_variant,genic_downstream_transcript_variant,non_coding_transcript_variant
                      Validated:
                      by frequency,by alfa,by cluster
                      MAF:
                      A=0./0 (ALFA)
                      A=0.000004/1 (TOPMED)
                      A=0.000014/2 (GnomAD)
                      HGVS:
                      NC_000011.10:g.13387063G>A, NC_000011.9:g.13408610G>A, NM_001178.6:c.*307G>A, NM_001178.5:c.*307G>A, NM_001178.4:c.*307G>A, XM_011520105.4:c.*307G>A, XM_011520105.3:c.*307G>A, XM_011520105.2:c.*307G>A, XM_011520105.1:c.*307G>A, XM_011520107.4:c.*307G>A, XM_011520107.3:c.*307G>A, XM_011520107.2:c.*307G>A, XM_011520107.1:c.*307G>A, XM_017017738.3:c.*307G>A, XM_017017738.2:c.*307G>A, XM_017017738.1:c.*307G>A, XM_017017739.3:c.*307G>A, XM_017017739.2:c.*307G>A, XM_017017739.1:c.*307G>A, NM_001030273.3:c.*307G>A, NM_001030273.2:c.*307G>A, NM_001030273.1:c.*307G>A, NM_001030272.3:c.*307G>A, NM_001030272.2:c.*307G>A, NM_001030272.1:c.*307G>A, NR_147789.2:n.2842G>A, NR_147789.1:n.2905G>A, NR_147787.2:n.2774G>A, NR_147787.1:n.2837G>A, NM_001351812.2:c.*307G>A, NM_001351812.1:c.*307G>A, NR_147790.2:n.2695G>A, NR_147790.1:n.2758G>A, NR_147791.2:n.2692G>A, NR_147791.1:n.2755G>A, NR_147788.2:n.2676G>A, NR_147788.1:n.2739G>A, NM_001351823.2:c.*307G>A, NM_001351823.1:c.*307G>A, NM_001351808.2:c.*307G>A, NM_001351808.1:c.*307G>A, NM_001351809.2:c.*307G>A, NM_001351809.1:c.*307G>A, NM_001351818.2:c.*307G>A, NM_001351818.1:c.*307G>A, NM_001351820.2:c.*307G>A, NM_001351820.1:c.*307G>A, NR_147785.2:n.2624G>A, NR_147785.1:n.2687G>A, NR_147786.2:n.2621G>A, NR_147786.1:n.2684G>A, NM_001351813.2:c.*307G>A, NM_001351813.1:c.*307G>A, NM_001351816.2:c.*307G>A, NM_001351816.1:c.*307G>A, NM_001351814.2:c.*307G>A, NM_001351814.1:c.*307G>A, NM_001297724.2:c.*307G>A, NM_001297724.1:c.*307G>A, NM_001297719.2:c.*307G>A, NM_001297719.1:c.*307G>A, NM_001351807.2:c.*307G>A, NM_001351807.1:c.*307G>A, NM_001351819.2:c.*307G>A, NM_001351819.1:c.*307G>A, NM_001351821.2:c.*307G>A, NM_001351821.1:c.*307G>A, NM_001297722.2:c.*307G>A, NM_001297722.1:c.*307G>A, NM_001351811.2:c.*307G>A, NM_001351811.1:c.*307G>A, NM_001351805.2:c.*307G>A, NM_001351805.1:c.*307G>A, NM_001351806.2:c.*307G>A, NM_001351806.1:c.*307G>A, NM_001351822.2:c.*307G>A, NM_001351822.1:c.*307G>A, XM_011520109.2:c.*307G>A, XM_011520109.1:c.*307G>A, XM_017017741.2:c.*307G>A, XM_017017741.1:c.*307G>A, NM_001351824.2:c.*307G>A, NM_001351824.1:c.*307G>A, NM_001351815.2:c.*307G>A, NM_001351815.1:c.*307G>A, NM_001351810.2:c.*307G>A, NM_001351810.1:c.*307G>A, NM_001351817.2:c.*307G>A, NM_001351817.1:c.*307G>A, XM_047426956.1:c.*307G>A, NM_001351804.1:c.*307G>A, XM_024448522.1:c.*307G>A, XM_047426953.1:c.*307G>A, XM_047426955.1:c.*307G>A, XM_047426952.1:c.*307G>A, XM_047426954.1:c.*307G>A

                      11.

                      rs1480267514 [Homo sapiens]
                        Variant type:
                        SNV
                        Alleles:
                        C>T [Show Flanks]
                        Chromosome:
                        11:13365535 (GRCh38)
                        11:13387082 (GRCh37)
                        Canonical SPDI:
                        NC_000011.10:13365534:C:T
                        Gene:
                        ARNTL (Varview)
                        Functional Consequence:
                        5_prime_UTR_variant,synonymous_variant,coding_sequence_variant,non_coding_transcript_variant
                        Validated:
                        by frequency,by alfa,by cluster
                        MAF:
                        T=0.0002/1 (ALFA)
                        T=0.0002/1 (Estonian)
                        HGVS:
                        NC_000011.10:g.13365535C>T, NC_000011.9:g.13387082C>T, NM_001178.6:c.495C>T, NM_001178.5:c.495C>T, NM_001178.4:c.495C>T, XM_011520105.4:c.624C>T, XM_011520105.3:c.624C>T, XM_011520105.2:c.624C>T, XM_011520105.1:c.495C>T, XM_011520107.4:c.624C>T, XM_011520107.3:c.624C>T, XM_011520107.2:c.624C>T, XM_011520107.1:c.495C>T, XM_017017738.3:c.624C>T, XM_017017738.2:c.624C>T, XM_017017738.1:c.624C>T, XM_017017739.3:c.624C>T, XM_017017739.2:c.624C>T, XM_017017739.1:c.624C>T, NM_001030273.3:c.366C>T, NM_001030273.2:c.366C>T, NM_001030273.1:c.366C>T, NM_001030272.3:c.495C>T, NM_001030272.2:c.495C>T, NM_001030272.1:c.495C>T, NR_147789.2:n.907C>T, NR_147789.1:n.970C>T, NR_147787.2:n.836C>T, NR_147787.1:n.899C>T, NM_001351812.2:c.444C>T, NM_001351812.1:c.444C>T, NR_147790.2:n.907C>T, NR_147790.1:n.970C>T, NR_147791.2:n.907C>T, NR_147791.1:n.970C>T, NR_147788.2:n.891C>T, NR_147788.1:n.954C>T, NM_001351823.2:c.366C>T, NM_001351823.1:c.366C>T, NM_001351808.2:c.366C>T, NM_001351808.1:c.366C>T, NM_001351809.2:c.444C>T, NM_001351809.1:c.444C>T, NM_001351818.2:c.366C>T, NM_001351818.1:c.366C>T, NM_001351820.2:c.366C>T, NM_001351820.1:c.366C>T, NR_147785.2:n.836C>T, NR_147785.1:n.899C>T, NR_147786.2:n.836C>T, NR_147786.1:n.899C>T, NM_001351813.2:c.366C>T, NM_001351813.1:c.366C>T, NM_001351816.2:c.366C>T, NM_001351816.1:c.366C>T, NM_001351814.2:c.495C>T, NM_001351814.1:c.495C>T, NM_001297724.2:c.366C>T, NM_001297724.1:c.366C>T, NM_001297719.2:c.495C>T, NM_001297719.1:c.495C>T, NM_001351807.2:c.495C>T, NM_001351807.1:c.495C>T, NM_001351819.2:c.495C>T, NM_001351819.1:c.495C>T, NM_001351821.2:c.366C>T, NM_001351821.1:c.366C>T, NM_001297722.2:c.495C>T, NM_001297722.1:c.495C>T, NM_001351811.2:c.-177C>T, NM_001351811.1:c.-177C>T, NM_001351805.2:c.456C>T, NM_001351805.1:c.456C>T, NM_001351806.2:c.456C>T, NM_001351806.1:c.456C>T, NM_001351822.2:c.366C>T, NM_001351822.1:c.366C>T, XM_011520109.2:c.495C>T, XM_011520109.1:c.495C>T, XM_017017741.2:c.495C>T, XM_017017741.1:c.495C>T, NM_001351824.2:c.495C>T, NM_001351824.1:c.495C>T, NM_001351815.2:c.495C>T, NM_001351815.1:c.495C>T, NM_001351810.2:c.495C>T, NM_001351810.1:c.495C>T, NM_001351817.2:c.495C>T, NM_001351817.1:c.495C>T, XM_047426956.1:c.495C>T, NM_001351804.1:c.495C>T, XM_024448522.1:c.444C>T, XM_047426953.1:c.495C>T, XM_047426955.1:c.495C>T, XM_047426952.1:c.495C>T, XM_047426954.1:c.495C>T, XM_047426957.1:c.624C>T, XM_047426958.1:c.624C>T

                        12.

                        rs1479720523 [Homo sapiens]
                          Variant type:
                          SNV
                          Alleles:
                          C>G,T [Show Flanks]
                          Chromosome:
                          11:13378342 (GRCh38)
                          11:13399889 (GRCh37)
                          Canonical SPDI:
                          NC_000011.10:13378341:C:G,NC_000011.10:13378341:C:T
                          Gene:
                          ARNTL (Varview)
                          Functional Consequence:
                          synonymous_variant,non_coding_transcript_variant,genic_downstream_transcript_variant,coding_sequence_variant,missense_variant
                          Validated:
                          by frequency,by alfa,by cluster
                          MAF:
                          G=0./0 (ALFA)
                          G=0.000004/1 (TOPMED)
                          G=0.000007/1 (GnomAD)
                          T=0.000342/1 (KOREAN)
                          HGVS:
                          NC_000011.10:g.13378342C>G, NC_000011.10:g.13378342C>T, NC_000011.9:g.13399889C>G, NC_000011.9:g.13399889C>T, NM_001178.6:c.1417C>G, NM_001178.6:c.1417C>T, NM_001178.5:c.1417C>G, NM_001178.5:c.1417C>T, NM_001178.4:c.1417C>G, NM_001178.4:c.1417C>T, XM_011520105.4:c.1561C>G, XM_011520105.4:c.1561C>T, XM_011520105.3:c.1561C>G, XM_011520105.3:c.1561C>T, XM_011520105.2:c.1561C>G, XM_011520105.2:c.1561C>T, XM_011520105.1:c.1432C>G, XM_011520105.1:c.1432C>T, XM_011520107.4:c.1546C>G, XM_011520107.4:c.1546C>T, XM_011520107.3:c.1546C>G, XM_011520107.3:c.1546C>T, XM_011520107.2:c.1546C>G, XM_011520107.2:c.1546C>T, XM_011520107.1:c.1417C>G, XM_011520107.1:c.1417C>T, XM_017017738.3:c.1564C>G, XM_017017738.3:c.1564C>T, XM_017017738.2:c.1564C>G, XM_017017738.2:c.1564C>T, XM_017017738.1:c.1564C>G, XM_017017738.1:c.1564C>T, XM_017017739.3:c.1549C>G, XM_017017739.3:c.1549C>T, XM_017017739.2:c.1549C>G, XM_017017739.2:c.1549C>T, XM_017017739.1:c.1549C>G, XM_017017739.1:c.1549C>T, NM_001030273.3:c.1288C>G, NM_001030273.3:c.1288C>T, NM_001030273.2:c.1288C>G, NM_001030273.2:c.1288C>T, NM_001030273.1:c.1288C>G, NM_001030273.1:c.1288C>T, NM_001030272.3:c.1417C>G, NM_001030272.3:c.1417C>T, NM_001030272.2:c.1417C>G, NM_001030272.2:c.1417C>T, NM_001030272.1:c.1417C>G, NM_001030272.1:c.1417C>T, NR_147789.2:n.1829C>G, NR_147789.2:n.1829C>T, NR_147789.1:n.1892C>G, NR_147789.1:n.1892C>T, NR_147787.2:n.1761C>G, NR_147787.2:n.1761C>T, NR_147787.1:n.1824C>G, NR_147787.1:n.1824C>T, NM_001351812.2:c.1369C>G, NM_001351812.2:c.1369C>T, NM_001351812.1:c.1369C>G, NM_001351812.1:c.1369C>T, NR_147790.2:n.1927C>G, NR_147790.2:n.1927C>T, NR_147790.1:n.1990C>G, NR_147790.1:n.1990C>T, NR_147791.2:n.1924C>G, NR_147791.2:n.1924C>T, NR_147791.1:n.1987C>G, NR_147791.1:n.1987C>T, NR_147788.2:n.1908C>G, NR_147788.2:n.1908C>T, NR_147788.1:n.1971C>G, NR_147788.1:n.1971C>T, NM_001351823.2:c.1306C>G, NM_001351823.2:c.1306C>T, NM_001351823.1:c.1306C>G, NM_001351823.1:c.1306C>T, NM_001351808.2:c.1291C>G, NM_001351808.2:c.1291C>T, NM_001351808.1:c.1291C>G, NM_001351808.1:c.1291C>T, NM_001351809.2:c.1369C>G, NM_001351809.2:c.1369C>T, NM_001351809.1:c.1369C>G, NM_001351809.1:c.1369C>T, NM_001351818.2:c.1288C>G, NM_001351818.2:c.1288C>T, NM_001351818.1:c.1288C>G, NM_001351818.1:c.1288C>T, NM_001351820.2:c.1291C>G, NM_001351820.2:c.1291C>T, NM_001351820.1:c.1291C>G, NM_001351820.1:c.1291C>T, NR_147785.2:n.1856C>G, NR_147785.2:n.1856C>T, NR_147785.1:n.1919C>G, NR_147785.1:n.1919C>T, NR_147786.2:n.1853C>G, NR_147786.2:n.1853C>T, NR_147786.1:n.1916C>G, NR_147786.1:n.1916C>T, NM_001351813.2:c.1303C>G, NM_001351813.2:c.1303C>T, NM_001351813.1:c.1303C>G, NM_001351813.1:c.1303C>T, NM_001351816.2:c.1291C>G, NM_001351816.2:c.1291C>T, NM_001351816.1:c.1291C>G, NM_001351816.1:c.1291C>T, NM_001351814.2:c.1435C>G, NM_001351814.2:c.1435C>T, NM_001351814.1:c.1435C>G, NM_001351814.1:c.1435C>T, NM_001297724.2:c.1291C>G, NM_001297724.2:c.1291C>T, NM_001297724.1:c.1291C>G, NM_001297724.1:c.1291C>T, NM_001297719.2:c.1420C>G, NM_001297719.2:c.1420C>T, NM_001297719.1:c.1420C>G, NM_001297719.1:c.1420C>T, NM_001351807.2:c.1435C>G, NM_001351807.2:c.1435C>T, NM_001351807.1:c.1435C>G, NM_001351807.1:c.1435C>T, NM_001351819.2:c.1432C>G, NM_001351819.2:c.1432C>T, NM_001351819.1:c.1432C>G, NM_001351819.1:c.1432C>T, NM_001351821.2:c.1291C>G, NM_001351821.2:c.1291C>T, NM_001351821.1:c.1291C>G, NM_001351821.1:c.1291C>T, NM_001297722.2:c.1420C>G, NM_001297722.2:c.1420C>T, NM_001297722.1:c.1420C>G, NM_001297722.1:c.1420C>T, NM_001351811.2:c.670C>G, NM_001351811.2:c.670C>T, NM_001351811.1:c.670C>G, NM_001351811.1:c.670C>T, NM_001351805.2:c.1381C>G, NM_001351805.2:c.1381C>T, NM_001351805.1:c.1381C>G, NM_001351805.1:c.1381C>T, NM_001351806.2:c.1378C>G, NM_001351806.2:c.1378C>T, NM_001351806.1:c.1378C>G, NM_001351806.1:c.1378C>T, NM_001351822.2:c.1291C>G, NM_001351822.2:c.1291C>T, NM_001351822.1:c.1291C>G, NM_001351822.1:c.1291C>T, XM_011520109.2:c.1435C>G, XM_011520109.2:c.1435C>T, XM_011520109.1:c.1435C>G, XM_011520109.1:c.1435C>T, XM_017017741.2:c.1432C>G, XM_017017741.2:c.1432C>T, XM_017017741.1:c.1432C>G, XM_017017741.1:c.1432C>T, NM_001351824.2:c.1420C>G, NM_001351824.2:c.1420C>T, NM_001351824.1:c.1420C>G, NM_001351824.1:c.1420C>T, NM_001351815.2:c.1417C>G, NM_001351815.2:c.1417C>T, NM_001351815.1:c.1417C>G, NM_001351815.1:c.1417C>T, NM_001351810.2:c.1066C>G, NM_001351810.2:c.1066C>T, NM_001351810.1:c.1066C>G, NM_001351810.1:c.1066C>T, NM_001351817.2:c.1066C>G, NM_001351817.2:c.1066C>T, NM_001351817.1:c.1066C>G, NM_001351817.1:c.1066C>T, XM_047426956.1:c.1435C>G, XM_047426956.1:c.1435C>T, NM_001351804.1:c.1417C>G, NM_001351804.1:c.1417C>T, XM_024448522.1:c.1369C>G, XM_024448522.1:c.1369C>T, XM_047426953.1:c.1435C>G, XM_047426953.1:c.1435C>T, XM_047426955.1:c.1435C>G, XM_047426955.1:c.1435C>T, XM_047426952.1:c.1435C>G, XM_047426952.1:c.1435C>T, XM_047426954.1:c.1435C>G, XM_047426954.1:c.1435C>T, XM_047426957.1:c.1644C>G, XM_047426957.1:c.1644C>T, NP_001169.3:p.Pro473Ala, NP_001169.3:p.Pro473Ser, XP_011518407.2:p.Pro521Ala, XP_011518407.2:p.Pro521Ser, XP_011518409.2:p.Pro516Ala, XP_011518409.2:p.Pro516Ser, XP_016873227.1:p.Pro522Ala, XP_016873227.1:p.Pro522Ser, XP_016873228.1:p.Pro517Ala, XP_016873228.1:p.Pro517Ser, NP_001025444.1:p.Pro430Ala, NP_001025444.1:p.Pro430Ser, NP_001025443.1:p.Pro473Ala, NP_001025443.1:p.Pro473Ser, NP_001338741.1:p.Pro457Ala, NP_001338741.1:p.Pro457Ser, NP_001338752.1:p.Pro436Ala, NP_001338752.1:p.Pro436Ser, NP_001338737.1:p.Pro431Ala, NP_001338737.1:p.Pro431Ser, NP_001338738.1:p.Pro457Ala, NP_001338738.1:p.Pro457Ser, NP_001338747.1:p.Pro430Ala, NP_001338747.1:p.Pro430Ser, NP_001338749.1:p.Pro431Ala, NP_001338749.1:p.Pro431Ser, NP_001338742.1:p.Pro435Ala, NP_001338742.1:p.Pro435Ser, NP_001338745.1:p.Pro431Ala, NP_001338745.1:p.Pro431Ser, NP_001338743.1:p.Pro479Ala, NP_001338743.1:p.Pro479Ser, NP_001284653.1:p.Pro431Ala, NP_001284653.1:p.Pro431Ser, NP_001284648.1:p.Pro474Ala, NP_001284648.1:p.Pro474Ser, NP_001338736.1:p.Pro479Ala, NP_001338736.1:p.Pro479Ser, NP_001338748.1:p.Pro478Ala, NP_001338748.1:p.Pro478Ser, NP_001338750.1:p.Pro431Ala, NP_001338750.1:p.Pro431Ser, NP_001284651.1:p.Pro474Ala, NP_001284651.1:p.Pro474Ser, NP_001338740.1:p.Pro224Ala, NP_001338740.1:p.Pro224Ser, NP_001338734.1:p.Pro461Ala, NP_001338734.1:p.Pro461Ser, NP_001338735.1:p.Pro460Ala, NP_001338735.1:p.Pro460Ser, NP_001338751.1:p.Pro431Ala, NP_001338751.1:p.Pro431Ser, XP_011518411.1:p.Pro479Ala, XP_011518411.1:p.Pro479Ser, XP_016873230.1:p.Pro478Ala, XP_016873230.1:p.Pro478Ser, NP_001338753.1:p.Pro474Ala, NP_001338753.1:p.Pro474Ser, NP_001338744.1:p.Pro473Ala, NP_001338744.1:p.Pro473Ser, NP_001338739.1:p.Pro356Ala, NP_001338739.1:p.Pro356Ser, NP_001338746.1:p.Pro356Ala, NP_001338746.1:p.Pro356Ser, XP_047282912.1:p.Pro479Ala, XP_047282912.1:p.Pro479Ser, NP_001338733.1:p.Pro473Ala, NP_001338733.1:p.Pro473Ser, XP_024304290.1:p.Pro457Ala, XP_024304290.1:p.Pro457Ser, XP_047282909.1:p.Pro479Ala, XP_047282909.1:p.Pro479Ser, XP_047282911.1:p.Pro479Ala, XP_047282911.1:p.Pro479Ser, XP_047282908.1:p.Pro479Ala, XP_047282908.1:p.Pro479Ser, XP_047282910.1:p.Pro479Ala, XP_047282910.1:p.Pro479Ser

                          13.

                          rs1477312788 [Homo sapiens]
                            Variant type:
                            SNV
                            Alleles:
                            A>G [Show Flanks]
                            Chromosome:
                            11:13387225 (GRCh38)
                            11:13408772 (GRCh37)
                            Canonical SPDI:
                            NC_000011.10:13387224:A:G
                            Gene:
                            ARNTL (Varview)
                            Functional Consequence:
                            3_prime_UTR_variant,genic_downstream_transcript_variant,non_coding_transcript_variant
                            Validated:
                            by frequency,by alfa
                            MAF:
                            G=0./0 (ALFA)
                            G=0.000008/2 (TOPMED)
                            HGVS:
                            NC_000011.10:g.13387225A>G, NC_000011.9:g.13408772A>G, NM_001178.6:c.*469A>G, NM_001178.5:c.*469A>G, NM_001178.4:c.*469A>G, XM_011520105.4:c.*469A>G, XM_011520105.3:c.*469A>G, XM_011520105.2:c.*469A>G, XM_011520105.1:c.*469A>G, XM_011520107.4:c.*469A>G, XM_011520107.3:c.*469A>G, XM_011520107.2:c.*469A>G, XM_011520107.1:c.*469A>G, XM_017017738.3:c.*469A>G, XM_017017738.2:c.*469A>G, XM_017017738.1:c.*469A>G, XM_017017739.3:c.*469A>G, XM_017017739.2:c.*469A>G, XM_017017739.1:c.*469A>G, NM_001030273.3:c.*469A>G, NM_001030273.2:c.*469A>G, NM_001030273.1:c.*469A>G, NM_001030272.3:c.*469A>G, NM_001030272.2:c.*469A>G, NM_001030272.1:c.*469A>G, NR_147789.2:n.3004A>G, NR_147789.1:n.3067A>G, NR_147787.2:n.2936A>G, NR_147787.1:n.2999A>G, NM_001351812.2:c.*469A>G, NM_001351812.1:c.*469A>G, NR_147790.2:n.2857A>G, NR_147790.1:n.2920A>G, NR_147791.2:n.2854A>G, NR_147791.1:n.2917A>G, NR_147788.2:n.2838A>G, NR_147788.1:n.2901A>G, NM_001351823.2:c.*469A>G, NM_001351823.1:c.*469A>G, NM_001351808.2:c.*469A>G, NM_001351808.1:c.*469A>G, NM_001351809.2:c.*469A>G, NM_001351809.1:c.*469A>G, NM_001351818.2:c.*469A>G, NM_001351818.1:c.*469A>G, NM_001351820.2:c.*469A>G, NM_001351820.1:c.*469A>G, NR_147785.2:n.2786A>G, NR_147785.1:n.2849A>G, NR_147786.2:n.2783A>G, NR_147786.1:n.2846A>G, NM_001351813.2:c.*469A>G, NM_001351813.1:c.*469A>G, NM_001351816.2:c.*469A>G, NM_001351816.1:c.*469A>G, NM_001351814.2:c.*469A>G, NM_001351814.1:c.*469A>G, NM_001297724.2:c.*469A>G, NM_001297724.1:c.*469A>G, NM_001297719.2:c.*469A>G, NM_001297719.1:c.*469A>G, NM_001351807.2:c.*469A>G, NM_001351807.1:c.*469A>G, NM_001351819.2:c.*469A>G, NM_001351819.1:c.*469A>G, NM_001351821.2:c.*469A>G, NM_001351821.1:c.*469A>G, NM_001297722.2:c.*469A>G, NM_001297722.1:c.*469A>G, NM_001351811.2:c.*469A>G, NM_001351811.1:c.*469A>G, NM_001351805.2:c.*469A>G, NM_001351805.1:c.*469A>G, NM_001351806.2:c.*469A>G, NM_001351806.1:c.*469A>G, NM_001351822.2:c.*469A>G, NM_001351822.1:c.*469A>G, XM_011520109.2:c.*469A>G, XM_011520109.1:c.*469A>G, XM_017017741.2:c.*469A>G, XM_017017741.1:c.*469A>G, NM_001351824.2:c.*469A>G, NM_001351824.1:c.*469A>G, NM_001351815.2:c.*469A>G, NM_001351815.1:c.*469A>G, NM_001351810.2:c.*469A>G, NM_001351810.1:c.*469A>G, NM_001351817.2:c.*469A>G, NM_001351817.1:c.*469A>G, XM_047426956.1:c.*469A>G, NM_001351804.1:c.*469A>G, XM_024448522.1:c.*469A>G, XM_047426953.1:c.*469A>G, XM_047426955.1:c.*469A>G, XM_047426952.1:c.*469A>G, XM_047426954.1:c.*469A>G

                            14.

                            rs1476924317 [Homo sapiens]
                              Variant type:
                              SNV
                              Alleles:
                              C>T [Show Flanks]
                              Chromosome:
                              11:13387252 (GRCh38)
                              11:13408799 (GRCh37)
                              Canonical SPDI:
                              NC_000011.10:13387251:C:T
                              Gene:
                              ARNTL (Varview)
                              Functional Consequence:
                              3_prime_UTR_variant,genic_downstream_transcript_variant,non_coding_transcript_variant
                              Validated:
                              by frequency,by alfa,by cluster
                              MAF:
                              T=0./0 (ALFA)
                              T=0.000007/1 (GnomAD)
                              T=0.000015/4 (TOPMED)
                              HGVS:
                              NC_000011.10:g.13387252C>T, NC_000011.9:g.13408799C>T, NM_001178.6:c.*496C>T, NM_001178.5:c.*496C>T, NM_001178.4:c.*496C>T, XM_011520105.4:c.*496C>T, XM_011520105.3:c.*496C>T, XM_011520105.2:c.*496C>T, XM_011520105.1:c.*496C>T, XM_011520107.4:c.*496C>T, XM_011520107.3:c.*496C>T, XM_011520107.2:c.*496C>T, XM_011520107.1:c.*496C>T, XM_017017738.3:c.*496C>T, XM_017017738.2:c.*496C>T, XM_017017738.1:c.*496C>T, XM_017017739.3:c.*496C>T, XM_017017739.2:c.*496C>T, XM_017017739.1:c.*496C>T, NM_001030273.3:c.*496C>T, NM_001030273.2:c.*496C>T, NM_001030273.1:c.*496C>T, NM_001030272.3:c.*496C>T, NM_001030272.2:c.*496C>T, NM_001030272.1:c.*496C>T, NR_147789.2:n.3031C>T, NR_147789.1:n.3094C>T, NR_147787.2:n.2963C>T, NR_147787.1:n.3026C>T, NM_001351812.2:c.*496C>T, NM_001351812.1:c.*496C>T, NR_147790.2:n.2884C>T, NR_147790.1:n.2947C>T, NR_147791.2:n.2881C>T, NR_147791.1:n.2944C>T, NR_147788.2:n.2865C>T, NR_147788.1:n.2928C>T, NM_001351823.2:c.*496C>T, NM_001351823.1:c.*496C>T, NM_001351808.2:c.*496C>T, NM_001351808.1:c.*496C>T, NM_001351809.2:c.*496C>T, NM_001351809.1:c.*496C>T, NM_001351818.2:c.*496C>T, NM_001351818.1:c.*496C>T, NM_001351820.2:c.*496C>T, NM_001351820.1:c.*496C>T, NR_147785.2:n.2813C>T, NR_147785.1:n.2876C>T, NR_147786.2:n.2810C>T, NR_147786.1:n.2873C>T, NM_001351813.2:c.*496C>T, NM_001351813.1:c.*496C>T, NM_001351816.2:c.*496C>T, NM_001351816.1:c.*496C>T, NM_001351814.2:c.*496C>T, NM_001351814.1:c.*496C>T, NM_001297724.2:c.*496C>T, NM_001297724.1:c.*496C>T, NM_001297719.2:c.*496C>T, NM_001297719.1:c.*496C>T, NM_001351807.2:c.*496C>T, NM_001351807.1:c.*496C>T, NM_001351819.2:c.*496C>T, NM_001351819.1:c.*496C>T, NM_001351821.2:c.*496C>T, NM_001351821.1:c.*496C>T, NM_001297722.2:c.*496C>T, NM_001297722.1:c.*496C>T, NM_001351811.2:c.*496C>T, NM_001351811.1:c.*496C>T, NM_001351805.2:c.*496C>T, NM_001351805.1:c.*496C>T, NM_001351806.2:c.*496C>T, NM_001351806.1:c.*496C>T, NM_001351822.2:c.*496C>T, NM_001351822.1:c.*496C>T, XM_011520109.2:c.*496C>T, XM_011520109.1:c.*496C>T, XM_017017741.2:c.*496C>T, XM_017017741.1:c.*496C>T, NM_001351824.2:c.*496C>T, NM_001351824.1:c.*496C>T, NM_001351815.2:c.*496C>T, NM_001351815.1:c.*496C>T, NM_001351810.2:c.*496C>T, NM_001351810.1:c.*496C>T, NM_001351817.2:c.*496C>T, NM_001351817.1:c.*496C>T, XM_047426956.1:c.*496C>T, NM_001351804.1:c.*496C>T, XM_024448522.1:c.*496C>T, XM_047426953.1:c.*496C>T, XM_047426955.1:c.*496C>T, XM_047426952.1:c.*496C>T, XM_047426954.1:c.*496C>T

                              15.

                              rs1474506574 [Homo sapiens]
                                Variant type:
                                SNV
                                Alleles:
                                T>A [Show Flanks]
                                Chromosome:
                                11:13374156 (GRCh38)
                                11:13395703 (GRCh37)
                                Canonical SPDI:
                                NC_000011.10:13374155:T:A
                                Gene:
                                ARNTL (Varview)
                                Functional Consequence:
                                intron_variant,non_coding_transcript_variant,genic_downstream_transcript_variant,coding_sequence_variant,missense_variant
                                Validated:
                                by frequency,by alfa,by cluster
                                MAF:
                                A=0./0 (ALFA)
                                A=0.000007/1 (GnomAD)
                                HGVS:
                                NC_000011.10:g.13374156T>A, NC_000011.9:g.13395703T>A, NM_001178.6:c.1126T>A, NM_001178.5:c.1126T>A, NM_001178.4:c.1126T>A, XM_011520105.4:c.1255T>A, XM_011520105.3:c.1255T>A, XM_011520105.2:c.1255T>A, XM_011520105.1:c.1126T>A, XM_011520107.4:c.1255T>A, XM_011520107.3:c.1255T>A, XM_011520107.2:c.1255T>A, XM_011520107.1:c.1126T>A, XM_017017738.3:c.1258T>A, XM_017017738.2:c.1258T>A, XM_017017738.1:c.1258T>A, XM_017017739.3:c.1258T>A, XM_017017739.2:c.1258T>A, XM_017017739.1:c.1258T>A, NM_001030273.3:c.997T>A, NM_001030273.2:c.997T>A, NM_001030273.1:c.997T>A, NM_001030272.3:c.1126T>A, NM_001030272.2:c.1126T>A, NM_001030272.1:c.1126T>A, NR_147789.2:n.1538T>A, NR_147789.1:n.1601T>A, NR_147787.2:n.1470T>A, NR_147787.1:n.1533T>A, NM_001351812.2:c.1078T>A, NM_001351812.1:c.1078T>A, NR_147790.2:n.1541T>A, NR_147790.1:n.1604T>A, NR_147791.2:n.1538T>A, NR_147791.1:n.1601T>A, NR_147788.2:n.1522T>A, NR_147788.1:n.1585T>A, NM_001351823.2:c.1000T>A, NM_001351823.1:c.1000T>A, NM_001351808.2:c.1000T>A, NM_001351808.1:c.1000T>A, NM_001351809.2:c.1078T>A, NM_001351809.1:c.1078T>A, NM_001351818.2:c.997T>A, NM_001351818.1:c.997T>A, NM_001351820.2:c.1000T>A, NM_001351820.1:c.1000T>A, NR_147785.2:n.1470T>A, NR_147785.1:n.1533T>A, NR_147786.2:n.1467T>A, NR_147786.1:n.1530T>A, NM_001351813.2:c.997T>A, NM_001351813.1:c.997T>A, NM_001351816.2:c.1000T>A, NM_001351816.1:c.1000T>A, NM_001351814.2:c.1129T>A, NM_001351814.1:c.1129T>A, NM_001297724.2:c.1000T>A, NM_001297724.1:c.1000T>A, NM_001297719.2:c.1129T>A, NM_001297719.1:c.1129T>A, NM_001351807.2:c.1129T>A, NM_001351807.1:c.1129T>A, NM_001351819.2:c.1126T>A, NM_001351819.1:c.1126T>A, NM_001351821.2:c.1000T>A, NM_001351821.1:c.1000T>A, NM_001297722.2:c.1129T>A, NM_001297722.1:c.1129T>A, NM_001351811.2:c.379T>A, NM_001351811.1:c.379T>A, NM_001351805.2:c.1090T>A, NM_001351805.1:c.1090T>A, NM_001351806.2:c.1087T>A, NM_001351806.1:c.1087T>A, NM_001351822.2:c.1000T>A, NM_001351822.1:c.1000T>A, XM_011520109.2:c.1129T>A, XM_011520109.1:c.1129T>A, XM_017017741.2:c.1126T>A, XM_017017741.1:c.1126T>A, NM_001351824.2:c.1129T>A, NM_001351824.1:c.1129T>A, NM_001351815.2:c.1126T>A, NM_001351815.1:c.1126T>A, XM_047426956.1:c.1129T>A, NM_001351804.1:c.1126T>A, XM_024448522.1:c.1078T>A, XM_047426953.1:c.1129T>A, XM_047426955.1:c.1129T>A, XM_047426952.1:c.1129T>A, XM_047426954.1:c.1129T>A, XM_047426957.1:c.1258T>A, NP_001169.3:p.Phe376Ile, XP_011518407.2:p.Phe419Ile, XP_011518409.2:p.Phe419Ile, XP_016873227.1:p.Phe420Ile, XP_016873228.1:p.Phe420Ile, NP_001025444.1:p.Phe333Ile, NP_001025443.1:p.Phe376Ile, NP_001338741.1:p.Phe360Ile, NP_001338752.1:p.Phe334Ile, NP_001338737.1:p.Phe334Ile, NP_001338738.1:p.Phe360Ile, NP_001338747.1:p.Phe333Ile, NP_001338749.1:p.Phe334Ile, NP_001338742.1:p.Phe333Ile, NP_001338745.1:p.Phe334Ile, NP_001338743.1:p.Phe377Ile, NP_001284653.1:p.Phe334Ile, NP_001284648.1:p.Phe377Ile, NP_001338736.1:p.Phe377Ile, NP_001338748.1:p.Phe376Ile, NP_001338750.1:p.Phe334Ile, NP_001284651.1:p.Phe377Ile, NP_001338740.1:p.Phe127Ile, NP_001338734.1:p.Phe364Ile, NP_001338735.1:p.Phe363Ile, NP_001338751.1:p.Phe334Ile, XP_011518411.1:p.Phe377Ile, XP_016873230.1:p.Phe376Ile, NP_001338753.1:p.Phe377Ile, NP_001338744.1:p.Phe376Ile, XP_047282912.1:p.Phe377Ile, NP_001338733.1:p.Phe376Ile, XP_024304290.1:p.Phe360Ile, XP_047282909.1:p.Phe377Ile, XP_047282911.1:p.Phe377Ile, XP_047282908.1:p.Phe377Ile, XP_047282910.1:p.Phe377Ile, XP_047282913.1:p.Phe420Ile

                                16.

                                rs1473717673 [Homo sapiens]
                                  Variant type:
                                  SNV
                                  Alleles:
                                  A>T [Show Flanks]
                                  Chromosome:
                                  11:13277024 (GRCh38)
                                  11:13298571 (GRCh37)
                                  Canonical SPDI:
                                  NC_000011.10:13277023:A:T
                                  Gene:
                                  ARNTL (Varview)
                                  Functional Consequence:
                                  5_prime_UTR_variant,upstream_transcript_variant,genic_upstream_transcript_variant
                                  Validated:
                                  by frequency,by alfa
                                  MAF:
                                  T=0./0 (ALFA)
                                  T=0.000007/1 (GnomAD)
                                  HGVS:

                                  17.

                                  rs1471310121 [Homo sapiens]
                                    Variant type:
                                    SNV
                                    Alleles:
                                    A>C,G [Show Flanks]
                                    Chromosome:
                                    11:13375632 (GRCh38)
                                    11:13397179 (GRCh37)
                                    Canonical SPDI:
                                    NC_000011.10:13375631:A:C,NC_000011.10:13375631:A:G
                                    Gene:
                                    ARNTL (Varview)
                                    Functional Consequence:
                                    missense_variant,coding_sequence_variant,genic_downstream_transcript_variant,non_coding_transcript_variant
                                    Validated:
                                    by frequency,by alfa,by cluster
                                    MAF:
                                    G=0./0 (ALFA)
                                    C=0.000014/2 (GnomAD)
                                    HGVS:
                                    NC_000011.10:g.13375632A>C, NC_000011.10:g.13375632A>G, NC_000011.9:g.13397179A>C, NC_000011.9:g.13397179A>G, NM_001178.6:c.1192A>C, NM_001178.6:c.1192A>G, NM_001178.5:c.1192A>C, NM_001178.5:c.1192A>G, NM_001178.4:c.1192A>C, NM_001178.4:c.1192A>G, XM_011520105.4:c.1321A>C, XM_011520105.4:c.1321A>G, XM_011520105.3:c.1321A>C, XM_011520105.3:c.1321A>G, XM_011520105.2:c.1321A>C, XM_011520105.2:c.1321A>G, XM_011520105.1:c.1192A>C, XM_011520105.1:c.1192A>G, XM_011520107.4:c.1321A>C, XM_011520107.4:c.1321A>G, XM_011520107.3:c.1321A>C, XM_011520107.3:c.1321A>G, XM_011520107.2:c.1321A>C, XM_011520107.2:c.1321A>G, XM_011520107.1:c.1192A>C, XM_011520107.1:c.1192A>G, XM_017017738.3:c.1324A>C, XM_017017738.3:c.1324A>G, XM_017017738.2:c.1324A>C, XM_017017738.2:c.1324A>G, XM_017017738.1:c.1324A>C, XM_017017738.1:c.1324A>G, XM_017017739.3:c.1324A>C, XM_017017739.3:c.1324A>G, XM_017017739.2:c.1324A>C, XM_017017739.2:c.1324A>G, XM_017017739.1:c.1324A>C, XM_017017739.1:c.1324A>G, NM_001030273.3:c.1063A>C, NM_001030273.3:c.1063A>G, NM_001030273.2:c.1063A>C, NM_001030273.2:c.1063A>G, NM_001030273.1:c.1063A>C, NM_001030273.1:c.1063A>G, NM_001030272.3:c.1192A>C, NM_001030272.3:c.1192A>G, NM_001030272.2:c.1192A>C, NM_001030272.2:c.1192A>G, NM_001030272.1:c.1192A>C, NM_001030272.1:c.1192A>G, NR_147789.2:n.1604A>C, NR_147789.2:n.1604A>G, NR_147789.1:n.1667A>C, NR_147789.1:n.1667A>G, NR_147787.2:n.1536A>C, NR_147787.2:n.1536A>G, NR_147787.1:n.1599A>C, NR_147787.1:n.1599A>G, NM_001351812.2:c.1144A>C, NM_001351812.2:c.1144A>G, NM_001351812.1:c.1144A>C, NM_001351812.1:c.1144A>G, NR_147790.2:n.1607A>C, NR_147790.2:n.1607A>G, NR_147790.1:n.1670A>C, NR_147790.1:n.1670A>G, NR_147791.2:n.1604A>C, NR_147791.2:n.1604A>G, NR_147791.1:n.1667A>C, NR_147791.1:n.1667A>G, NR_147788.2:n.1588A>C, NR_147788.2:n.1588A>G, NR_147788.1:n.1651A>C, NR_147788.1:n.1651A>G, NM_001351823.2:c.1066A>C, NM_001351823.2:c.1066A>G, NM_001351823.1:c.1066A>C, NM_001351823.1:c.1066A>G, NM_001351808.2:c.1066A>C, NM_001351808.2:c.1066A>G, NM_001351808.1:c.1066A>C, NM_001351808.1:c.1066A>G, NM_001351809.2:c.1144A>C, NM_001351809.2:c.1144A>G, NM_001351809.1:c.1144A>C, NM_001351809.1:c.1144A>G, NM_001351818.2:c.1063A>C, NM_001351818.2:c.1063A>G, NM_001351818.1:c.1063A>C, NM_001351818.1:c.1063A>G, NM_001351820.2:c.1066A>C, NM_001351820.2:c.1066A>G, NM_001351820.1:c.1066A>C, NM_001351820.1:c.1066A>G, NR_147785.2:n.1536A>C, NR_147785.2:n.1536A>G, NR_147785.1:n.1599A>C, NR_147785.1:n.1599A>G, NR_147786.2:n.1533A>C, NR_147786.2:n.1533A>G, NR_147786.1:n.1596A>C, NR_147786.1:n.1596A>G, NM_001351813.2:c.1063A>C, NM_001351813.2:c.1063A>G, NM_001351813.1:c.1063A>C, NM_001351813.1:c.1063A>G, NM_001351816.2:c.1066A>C, NM_001351816.2:c.1066A>G, NM_001351816.1:c.1066A>C, NM_001351816.1:c.1066A>G, NM_001351814.2:c.1195A>C, NM_001351814.2:c.1195A>G, NM_001351814.1:c.1195A>C, NM_001351814.1:c.1195A>G, NM_001297724.2:c.1066A>C, NM_001297724.2:c.1066A>G, NM_001297724.1:c.1066A>C, NM_001297724.1:c.1066A>G, NM_001297719.2:c.1195A>C, NM_001297719.2:c.1195A>G, NM_001297719.1:c.1195A>C, NM_001297719.1:c.1195A>G, NM_001351807.2:c.1195A>C, NM_001351807.2:c.1195A>G, NM_001351807.1:c.1195A>C, NM_001351807.1:c.1195A>G, NM_001351819.2:c.1192A>C, NM_001351819.2:c.1192A>G, NM_001351819.1:c.1192A>C, NM_001351819.1:c.1192A>G, NM_001351821.2:c.1066A>C, NM_001351821.2:c.1066A>G, NM_001351821.1:c.1066A>C, NM_001351821.1:c.1066A>G, NM_001297722.2:c.1195A>C, NM_001297722.2:c.1195A>G, NM_001297722.1:c.1195A>C, NM_001297722.1:c.1195A>G, NM_001351811.2:c.445A>C, NM_001351811.2:c.445A>G, NM_001351811.1:c.445A>C, NM_001351811.1:c.445A>G, NM_001351805.2:c.1156A>C, NM_001351805.2:c.1156A>G, NM_001351805.1:c.1156A>C, NM_001351805.1:c.1156A>G, NM_001351806.2:c.1153A>C, NM_001351806.2:c.1153A>G, NM_001351806.1:c.1153A>C, NM_001351806.1:c.1153A>G, NM_001351822.2:c.1066A>C, NM_001351822.2:c.1066A>G, NM_001351822.1:c.1066A>C, NM_001351822.1:c.1066A>G, XM_011520109.2:c.1195A>C, XM_011520109.2:c.1195A>G, XM_011520109.1:c.1195A>C, XM_011520109.1:c.1195A>G, XM_017017741.2:c.1192A>C, XM_017017741.2:c.1192A>G, XM_017017741.1:c.1192A>C, XM_017017741.1:c.1192A>G, NM_001351824.2:c.1195A>C, NM_001351824.2:c.1195A>G, NM_001351824.1:c.1195A>C, NM_001351824.1:c.1195A>G, NM_001351815.2:c.1192A>C, NM_001351815.2:c.1192A>G, NM_001351815.1:c.1192A>C, NM_001351815.1:c.1192A>G, NM_001351810.2:c.841A>C, NM_001351810.2:c.841A>G, NM_001351810.1:c.841A>C, NM_001351810.1:c.841A>G, NM_001351817.2:c.841A>C, NM_001351817.2:c.841A>G, NM_001351817.1:c.841A>C, NM_001351817.1:c.841A>G, XM_047426956.1:c.1195A>C, XM_047426956.1:c.1195A>G, NM_001351804.1:c.1192A>C, NM_001351804.1:c.1192A>G, XM_024448522.1:c.1144A>C, XM_024448522.1:c.1144A>G, XM_047426953.1:c.1195A>C, XM_047426953.1:c.1195A>G, XM_047426955.1:c.1195A>C, XM_047426955.1:c.1195A>G, XM_047426952.1:c.1195A>C, XM_047426952.1:c.1195A>G, XM_047426954.1:c.1195A>C, XM_047426954.1:c.1195A>G, XM_047426957.1:c.1324A>C, XM_047426957.1:c.1324A>G, NP_001169.3:p.Ile398Leu, NP_001169.3:p.Ile398Val, XP_011518407.2:p.Ile441Leu, XP_011518407.2:p.Ile441Val, XP_011518409.2:p.Ile441Leu, XP_011518409.2:p.Ile441Val, XP_016873227.1:p.Ile442Leu, XP_016873227.1:p.Ile442Val, XP_016873228.1:p.Ile442Leu, XP_016873228.1:p.Ile442Val, NP_001025444.1:p.Ile355Leu, NP_001025444.1:p.Ile355Val, NP_001025443.1:p.Ile398Leu, NP_001025443.1:p.Ile398Val, NP_001338741.1:p.Ile382Leu, NP_001338741.1:p.Ile382Val, NP_001338752.1:p.Ile356Leu, NP_001338752.1:p.Ile356Val, NP_001338737.1:p.Ile356Leu, NP_001338737.1:p.Ile356Val, NP_001338738.1:p.Ile382Leu, NP_001338738.1:p.Ile382Val, NP_001338747.1:p.Ile355Leu, NP_001338747.1:p.Ile355Val, NP_001338749.1:p.Ile356Leu, NP_001338749.1:p.Ile356Val, NP_001338742.1:p.Ile355Leu, NP_001338742.1:p.Ile355Val, NP_001338745.1:p.Ile356Leu, NP_001338745.1:p.Ile356Val, NP_001338743.1:p.Ile399Leu, NP_001338743.1:p.Ile399Val, NP_001284653.1:p.Ile356Leu, NP_001284653.1:p.Ile356Val, NP_001284648.1:p.Ile399Leu, NP_001284648.1:p.Ile399Val, NP_001338736.1:p.Ile399Leu, NP_001338736.1:p.Ile399Val, NP_001338748.1:p.Ile398Leu, NP_001338748.1:p.Ile398Val, NP_001338750.1:p.Ile356Leu, NP_001338750.1:p.Ile356Val, NP_001284651.1:p.Ile399Leu, NP_001284651.1:p.Ile399Val, NP_001338740.1:p.Ile149Leu, NP_001338740.1:p.Ile149Val, NP_001338734.1:p.Ile386Leu, NP_001338734.1:p.Ile386Val, NP_001338735.1:p.Ile385Leu, NP_001338735.1:p.Ile385Val, NP_001338751.1:p.Ile356Leu, NP_001338751.1:p.Ile356Val, XP_011518411.1:p.Ile399Leu, XP_011518411.1:p.Ile399Val, XP_016873230.1:p.Ile398Leu, XP_016873230.1:p.Ile398Val, NP_001338753.1:p.Ile399Leu, NP_001338753.1:p.Ile399Val, NP_001338744.1:p.Ile398Leu, NP_001338744.1:p.Ile398Val, NP_001338739.1:p.Ile281Leu, NP_001338739.1:p.Ile281Val, NP_001338746.1:p.Ile281Leu, NP_001338746.1:p.Ile281Val, XP_047282912.1:p.Ile399Leu, XP_047282912.1:p.Ile399Val, NP_001338733.1:p.Ile398Leu, NP_001338733.1:p.Ile398Val, XP_024304290.1:p.Ile382Leu, XP_024304290.1:p.Ile382Val, XP_047282909.1:p.Ile399Leu, XP_047282909.1:p.Ile399Val, XP_047282911.1:p.Ile399Leu, XP_047282911.1:p.Ile399Val, XP_047282908.1:p.Ile399Leu, XP_047282908.1:p.Ile399Val, XP_047282910.1:p.Ile399Leu, XP_047282910.1:p.Ile399Val, XP_047282913.1:p.Ile442Leu, XP_047282913.1:p.Ile442Val

                                    18.

                                    rs1469622122 [Homo sapiens]
                                      Variant type:
                                      SNV
                                      Alleles:
                                      A>C [Show Flanks]
                                      Chromosome:
                                      11:13354338 (GRCh38)
                                      11:13375885 (GRCh37)
                                      Canonical SPDI:
                                      NC_000011.10:13354337:A:C
                                      Gene:
                                      ARNTL (Varview), LOC124902636 (Varview)
                                      Functional Consequence:
                                      500B_downstream_variant,non_coding_transcript_variant,synonymous_variant,downstream_transcript_variant,5_prime_UTR_variant,upstream_transcript_variant,genic_upstream_transcript_variant,coding_sequence_variant
                                      Validated:
                                      by frequency,by alfa,by cluster
                                      MAF:
                                      C=0./0 (ALFA)
                                      C=0.000007/1 (GnomAD)
                                      C=0.000023/6 (TOPMED)
                                      HGVS:
                                      NC_000011.10:g.13354338A>C, NC_000011.9:g.13375885A>C, NM_001178.6:c.30A>C, NM_001178.5:c.30A>C, NM_001178.4:c.30A>C, XM_011520105.4:c.159A>C, XM_011520105.3:c.159A>C, XM_011520105.2:c.159A>C, XM_011520105.1:c.30A>C, XM_011520107.4:c.159A>C, XM_011520107.3:c.159A>C, XM_011520107.2:c.159A>C, XM_011520107.1:c.30A>C, XM_017017738.3:c.159A>C, XM_017017738.2:c.159A>C, XM_017017738.1:c.159A>C, XM_017017739.3:c.159A>C, XM_017017739.2:c.159A>C, XM_017017739.1:c.159A>C, NM_001030273.3:c.-171A>C, NM_001030273.2:c.-171A>C, NM_001030273.1:c.-171A>C, NM_001030272.3:c.30A>C, NM_001030272.2:c.30A>C, NM_001030272.1:c.30A>C, NR_147789.2:n.371A>C, NR_147789.1:n.434A>C, NR_147787.2:n.371A>C, NR_147787.1:n.434A>C, NM_001351812.2:c.-146A>C, NM_001351812.1:c.-146A>C, NR_147790.2:n.371A>C, NR_147790.1:n.434A>C, NR_147791.2:n.371A>C, NR_147791.1:n.434A>C, NR_147788.2:n.426A>C, NR_147788.1:n.489A>C, NM_001351823.2:c.-171A>C, NM_001351823.1:c.-171A>C, NM_001351808.2:c.-171A>C, NM_001351808.1:c.-171A>C, NM_001351809.2:c.-146A>C, NM_001351809.1:c.-146A>C, NM_001351818.2:c.-171A>C, NM_001351818.1:c.-171A>C, NM_001351820.2:c.-164A>C, NM_001351820.1:c.-164A>C, NR_147785.2:n.371A>C, NR_147785.1:n.434A>C, NR_147786.2:n.371A>C, NR_147786.1:n.434A>C, NM_001351813.2:c.-171A>C, NM_001351813.1:c.-171A>C, NM_001351816.2:c.-171A>C, NM_001351816.1:c.-171A>C, NM_001351814.2:c.30A>C, NM_001351814.1:c.30A>C, NM_001297724.2:c.-164A>C, NM_001297724.1:c.-164A>C, NM_001297719.2:c.30A>C, NM_001297719.1:c.30A>C, NM_001351807.2:c.30A>C, NM_001351807.1:c.30A>C, NM_001351819.2:c.30A>C, NM_001351819.1:c.30A>C, NM_001351821.2:c.-171A>C, NM_001351821.1:c.-171A>C, NM_001297722.2:c.30A>C, NM_001297722.1:c.30A>C, NM_001351811.2:c.-713A>C, NM_001351811.1:c.-713A>C, NM_001351805.2:c.30A>C, NM_001351805.1:c.30A>C, NM_001351806.2:c.30A>C, NM_001351806.1:c.30A>C, NM_001351822.2:c.-171A>C, NM_001351822.1:c.-171A>C, XM_011520109.2:c.30A>C, XM_011520109.1:c.30A>C, XM_017017741.2:c.30A>C, XM_017017741.1:c.30A>C, NM_001351824.2:c.30A>C, NM_001351824.1:c.30A>C, NM_001351815.2:c.30A>C, NM_001351815.1:c.30A>C, NM_001351810.2:c.30A>C, NM_001351810.1:c.30A>C, NM_001351817.2:c.30A>C, NM_001351817.1:c.30A>C, XM_047426956.1:c.30A>C, NM_001351804.1:c.30A>C, XM_047426953.1:c.30A>C, XM_047426955.1:c.30A>C, XM_047426952.1:c.30A>C, XM_047426954.1:c.30A>C, XM_047426957.1:c.159A>C, XM_047426958.1:c.159A>C

                                      19.

                                      rs1469394014 [Homo sapiens]
                                        Variant type:
                                        SNV
                                        Alleles:
                                        T>C [Show Flanks]
                                        Chromosome:
                                        11:13376648 (GRCh38)
                                        11:13398195 (GRCh37)
                                        Canonical SPDI:
                                        NC_000011.10:13376647:T:C
                                        Gene:
                                        ARNTL (Varview)
                                        Functional Consequence:
                                        coding_sequence_variant,missense_variant,genic_downstream_transcript_variant,non_coding_transcript_variant
                                        Validated:
                                        by frequency,by alfa,by cluster
                                        MAF:
                                        C=0./0 (ALFA)
                                        C=0.000004/1 (TOPMED)
                                        C=0.000008/2 (GnomAD_exomes)
                                        HGVS:
                                        NC_000011.10:g.13376648T>C, NC_000011.9:g.13398195T>C, NM_001178.6:c.1331T>C, NM_001178.5:c.1331T>C, NM_001178.4:c.1331T>C, XM_011520105.4:c.1460T>C, XM_011520105.3:c.1460T>C, XM_011520105.2:c.1460T>C, XM_011520105.1:c.1331T>C, XM_011520107.4:c.1460T>C, XM_011520107.3:c.1460T>C, XM_011520107.2:c.1460T>C, XM_011520107.1:c.1331T>C, XM_017017738.3:c.1463T>C, XM_017017738.2:c.1463T>C, XM_017017738.1:c.1463T>C, XM_017017739.3:c.1463T>C, XM_017017739.2:c.1463T>C, XM_017017739.1:c.1463T>C, NM_001030273.3:c.1202T>C, NM_001030273.2:c.1202T>C, NM_001030273.1:c.1202T>C, NM_001030272.3:c.1331T>C, NM_001030272.2:c.1331T>C, NM_001030272.1:c.1331T>C, NR_147789.2:n.1743T>C, NR_147789.1:n.1806T>C, NR_147787.2:n.1675T>C, NR_147787.1:n.1738T>C, NM_001351812.2:c.1283T>C, NM_001351812.1:c.1283T>C, NR_147790.2:n.1841T>C, NR_147790.1:n.1904T>C, NR_147791.2:n.1838T>C, NR_147791.1:n.1901T>C, NR_147788.2:n.1822T>C, NR_147788.1:n.1885T>C, NM_001351823.2:c.1205T>C, NM_001351823.1:c.1205T>C, NM_001351808.2:c.1205T>C, NM_001351808.1:c.1205T>C, NM_001351809.2:c.1283T>C, NM_001351809.1:c.1283T>C, NM_001351818.2:c.1202T>C, NM_001351818.1:c.1202T>C, NM_001351820.2:c.1205T>C, NM_001351820.1:c.1205T>C, NR_147785.2:n.1770T>C, NR_147785.1:n.1833T>C, NR_147786.2:n.1767T>C, NR_147786.1:n.1830T>C, NM_001351813.2:c.1202T>C, NM_001351813.1:c.1202T>C, NM_001351816.2:c.1205T>C, NM_001351816.1:c.1205T>C, NM_001351814.2:c.1334T>C, NM_001351814.1:c.1334T>C, NM_001297724.2:c.1205T>C, NM_001297724.1:c.1205T>C, NM_001297719.2:c.1334T>C, NM_001297719.1:c.1334T>C, NM_001351807.2:c.1334T>C, NM_001351807.1:c.1334T>C, NM_001351819.2:c.1331T>C, NM_001351819.1:c.1331T>C, NM_001351821.2:c.1205T>C, NM_001351821.1:c.1205T>C, NM_001297722.2:c.1334T>C, NM_001297722.1:c.1334T>C, NM_001351811.2:c.584T>C, NM_001351811.1:c.584T>C, NM_001351805.2:c.1295T>C, NM_001351805.1:c.1295T>C, NM_001351806.2:c.1292T>C, NM_001351806.1:c.1292T>C, NM_001351822.2:c.1205T>C, NM_001351822.1:c.1205T>C, XM_011520109.2:c.1334T>C, XM_011520109.1:c.1334T>C, XM_017017741.2:c.1331T>C, XM_017017741.1:c.1331T>C, NM_001351824.2:c.1334T>C, NM_001351824.1:c.1334T>C, NM_001351815.2:c.1331T>C, NM_001351815.1:c.1331T>C, NM_001351810.2:c.980T>C, NM_001351810.1:c.980T>C, NM_001351817.2:c.980T>C, NM_001351817.1:c.980T>C, XM_047426956.1:c.1334T>C, NM_001351804.1:c.1331T>C, XM_024448522.1:c.1283T>C, XM_047426953.1:c.1334T>C, XM_047426955.1:c.1334T>C, XM_047426952.1:c.1334T>C, XM_047426954.1:c.1334T>C, XM_047426957.1:c.1558T>C, NP_001169.3:p.Val444Ala, XP_011518407.2:p.Val487Ala, XP_011518409.2:p.Val487Ala, XP_016873227.1:p.Val488Ala, XP_016873228.1:p.Val488Ala, NP_001025444.1:p.Val401Ala, NP_001025443.1:p.Val444Ala, NP_001338741.1:p.Val428Ala, NP_001338752.1:p.Val402Ala, NP_001338737.1:p.Val402Ala, NP_001338738.1:p.Val428Ala, NP_001338747.1:p.Val401Ala, NP_001338749.1:p.Val402Ala, NP_001338742.1:p.Val401Ala, NP_001338745.1:p.Val402Ala, NP_001338743.1:p.Val445Ala, NP_001284653.1:p.Val402Ala, NP_001284648.1:p.Val445Ala, NP_001338736.1:p.Val445Ala, NP_001338748.1:p.Val444Ala, NP_001338750.1:p.Val402Ala, NP_001284651.1:p.Val445Ala, NP_001338740.1:p.Val195Ala, NP_001338734.1:p.Val432Ala, NP_001338735.1:p.Val431Ala, NP_001338751.1:p.Val402Ala, XP_011518411.1:p.Val445Ala, XP_016873230.1:p.Val444Ala, NP_001338753.1:p.Val445Ala, NP_001338744.1:p.Val444Ala, NP_001338739.1:p.Val327Ala, NP_001338746.1:p.Val327Ala, XP_047282912.1:p.Val445Ala, NP_001338733.1:p.Val444Ala, XP_024304290.1:p.Val428Ala, XP_047282909.1:p.Val445Ala, XP_047282911.1:p.Val445Ala, XP_047282908.1:p.Val445Ala, XP_047282910.1:p.Val445Ala, XP_047282913.1:p.Ser520Pro

                                        20.

                                        rs1467340502 [Homo sapiens]
                                          Variant type:
                                          SNV
                                          Alleles:
                                          A>G [Show Flanks]
                                          Chromosome:
                                          11:13354316 (GRCh38)
                                          11:13375863 (GRCh37)
                                          Canonical SPDI:
                                          NC_000011.10:13354315:A:G
                                          Gene:
                                          ARNTL (Varview), LOC124902636 (Varview)
                                          Functional Consequence:
                                          500B_downstream_variant,missense_variant,non_coding_transcript_variant,downstream_transcript_variant,5_prime_UTR_variant,upstream_transcript_variant,genic_upstream_transcript_variant,coding_sequence_variant
                                          Validated:
                                          by frequency,by cluster
                                          MAF:
                                          G=0.000004/1 (GnomAD_exomes)
                                          HGVS:
                                          NC_000011.10:g.13354316A>G, NC_000011.9:g.13375863A>G, NM_001178.6:c.8A>G, NM_001178.5:c.8A>G, NM_001178.4:c.8A>G, XM_011520105.4:c.137A>G, XM_011520105.3:c.137A>G, XM_011520105.2:c.137A>G, XM_011520105.1:c.8A>G, XM_011520107.4:c.137A>G, XM_011520107.3:c.137A>G, XM_011520107.2:c.137A>G, XM_011520107.1:c.8A>G, XM_017017738.3:c.137A>G, XM_017017738.2:c.137A>G, XM_017017738.1:c.137A>G, XM_017017739.3:c.137A>G, XM_017017739.2:c.137A>G, XM_017017739.1:c.137A>G, NM_001030273.3:c.-193A>G, NM_001030273.2:c.-193A>G, NM_001030273.1:c.-193A>G, NM_001030272.3:c.8A>G, NM_001030272.2:c.8A>G, NM_001030272.1:c.8A>G, NR_147789.2:n.349A>G, NR_147789.1:n.412A>G, NR_147787.2:n.349A>G, NR_147787.1:n.412A>G, NM_001351812.2:c.-168A>G, NM_001351812.1:c.-168A>G, NR_147790.2:n.349A>G, NR_147790.1:n.412A>G, NR_147791.2:n.349A>G, NR_147791.1:n.412A>G, NR_147788.2:n.404A>G, NR_147788.1:n.467A>G, NM_001351823.2:c.-193A>G, NM_001351823.1:c.-193A>G, NM_001351808.2:c.-193A>G, NM_001351808.1:c.-193A>G, NM_001351809.2:c.-168A>G, NM_001351809.1:c.-168A>G, NM_001351818.2:c.-193A>G, NM_001351818.1:c.-193A>G, NM_001351820.2:c.-186A>G, NM_001351820.1:c.-186A>G, NR_147785.2:n.349A>G, NR_147785.1:n.412A>G, NR_147786.2:n.349A>G, NR_147786.1:n.412A>G, NM_001351813.2:c.-193A>G, NM_001351813.1:c.-193A>G, NM_001351816.2:c.-193A>G, NM_001351816.1:c.-193A>G, NM_001351814.2:c.8A>G, NM_001351814.1:c.8A>G, NM_001297724.2:c.-186A>G, NM_001297724.1:c.-186A>G, NM_001297719.2:c.8A>G, NM_001297719.1:c.8A>G, NM_001351807.2:c.8A>G, NM_001351807.1:c.8A>G, NM_001351819.2:c.8A>G, NM_001351819.1:c.8A>G, NM_001351821.2:c.-193A>G, NM_001351821.1:c.-193A>G, NM_001297722.2:c.8A>G, NM_001297722.1:c.8A>G, NM_001351811.2:c.-735A>G, NM_001351811.1:c.-735A>G, NM_001351805.2:c.8A>G, NM_001351805.1:c.8A>G, NM_001351806.2:c.8A>G, NM_001351806.1:c.8A>G, NM_001351822.2:c.-193A>G, NM_001351822.1:c.-193A>G, XM_011520109.2:c.8A>G, XM_011520109.1:c.8A>G, XM_017017741.2:c.8A>G, XM_017017741.1:c.8A>G, NM_001351824.2:c.8A>G, NM_001351824.1:c.8A>G, NM_001351815.2:c.8A>G, NM_001351815.1:c.8A>G, NM_001351810.2:c.8A>G, NM_001351810.1:c.8A>G, NM_001351817.2:c.8A>G, NM_001351817.1:c.8A>G, XM_047426956.1:c.8A>G, NM_001351804.1:c.8A>G, XM_047426953.1:c.8A>G, XM_047426955.1:c.8A>G, XM_047426952.1:c.8A>G, XM_047426954.1:c.8A>G, XM_047426957.1:c.137A>G, XM_047426958.1:c.137A>G, NP_001169.3:p.Asp3Gly, XP_011518407.2:p.Asp46Gly, XP_011518409.2:p.Asp46Gly, XP_016873227.1:p.Asp46Gly, XP_016873228.1:p.Asp46Gly, NP_001025443.1:p.Asp3Gly, NP_001338743.1:p.Asp3Gly, NP_001284648.1:p.Asp3Gly, NP_001338736.1:p.Asp3Gly, NP_001338748.1:p.Asp3Gly, NP_001284651.1:p.Asp3Gly, NP_001338734.1:p.Asp3Gly, NP_001338735.1:p.Asp3Gly, XP_011518411.1:p.Asp3Gly, XP_016873230.1:p.Asp3Gly, NP_001338753.1:p.Asp3Gly, NP_001338744.1:p.Asp3Gly, NP_001338739.1:p.Asp3Gly, NP_001338746.1:p.Asp3Gly, XP_047282912.1:p.Asp3Gly, NP_001338733.1:p.Asp3Gly, XP_047282909.1:p.Asp3Gly, XP_047282911.1:p.Asp3Gly, XP_047282908.1:p.Asp3Gly, XP_047282910.1:p.Asp3Gly, XP_047282913.1:p.Asp46Gly, XP_047282914.1:p.Asp46Gly

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