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1.

rs1491495420 has merged into rs34047775 [Homo sapiens]
    Variant type:
    DELINS
    Alleles:
    TTTTTTTTTTTTT>-,T,TT,TTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
    Chromosome:
    18:62341846 (GRCh38)
    18:60009079 (GRCh37)
    Canonical SPDI:
    NC_000018.10:62341836:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000018.10:62341836:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000018.10:62341836:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000018.10:62341836:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000018.10:62341836:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000018.10:62341836:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000018.10:62341836:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000018.10:62341836:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000018.10:62341836:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000018.10:62341836:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000018.10:62341836:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:62341836:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:62341836:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:62341836:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:62341836:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:62341836:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:62341836:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:62341836:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:62341836:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:62341836:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:62341836:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:62341836:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:62341836:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:62341836:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:62341836:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:62341836:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
    Gene:
    TNFRSF11A (Varview)
    Functional Consequence:
    genic_upstream_transcript_variant,intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    TTTTTTTTTT=0./0 (ALFA)
    -=0.000004/1 (TOPMED)
    HGVS:
    NC_000018.10:g.62341846_62341858del, NC_000018.10:g.62341847_62341858del, NC_000018.10:g.62341848_62341858del, NC_000018.10:g.62341851_62341858del, NC_000018.10:g.62341853_62341858del, NC_000018.10:g.62341854_62341858del, NC_000018.10:g.62341855_62341858del, NC_000018.10:g.62341856_62341858del, NC_000018.10:g.62341857_62341858del, NC_000018.10:g.62341858del, NC_000018.10:g.62341858dup, NC_000018.10:g.62341857_62341858dup, NC_000018.10:g.62341856_62341858dup, NC_000018.10:g.62341855_62341858dup, NC_000018.10:g.62341854_62341858dup, NC_000018.10:g.62341853_62341858dup, NC_000018.10:g.62341852_62341858dup, NC_000018.10:g.62341851_62341858dup, NC_000018.10:g.62341850_62341858dup, NC_000018.10:g.62341849_62341858dup, NC_000018.10:g.62341848_62341858dup, NC_000018.10:g.62341847_62341858dup, NC_000018.10:g.62341844_62341858dup, NC_000018.10:g.62341842_62341858dup, NC_000018.10:g.62341841_62341858dup, NC_000018.10:g.62341858_62341859insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000018.9:g.60009079_60009091del, NC_000018.9:g.60009080_60009091del, NC_000018.9:g.60009081_60009091del, NC_000018.9:g.60009084_60009091del, NC_000018.9:g.60009086_60009091del, NC_000018.9:g.60009087_60009091del, NC_000018.9:g.60009088_60009091del, NC_000018.9:g.60009089_60009091del, NC_000018.9:g.60009090_60009091del, NC_000018.9:g.60009091del, NC_000018.9:g.60009091dup, NC_000018.9:g.60009090_60009091dup, NC_000018.9:g.60009089_60009091dup, NC_000018.9:g.60009088_60009091dup, NC_000018.9:g.60009087_60009091dup, NC_000018.9:g.60009086_60009091dup, NC_000018.9:g.60009085_60009091dup, NC_000018.9:g.60009084_60009091dup, NC_000018.9:g.60009083_60009091dup, NC_000018.9:g.60009082_60009091dup, NC_000018.9:g.60009081_60009091dup, NC_000018.9:g.60009080_60009091dup, NC_000018.9:g.60009077_60009091dup, NC_000018.9:g.60009075_60009091dup, NC_000018.9:g.60009074_60009091dup, NC_000018.9:g.60009091_60009092insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_008098.1:g.21532_21544del, NG_008098.1:g.21533_21544del, NG_008098.1:g.21534_21544del, NG_008098.1:g.21537_21544del, NG_008098.1:g.21539_21544del, NG_008098.1:g.21540_21544del, NG_008098.1:g.21541_21544del, NG_008098.1:g.21542_21544del, NG_008098.1:g.21543_21544del, NG_008098.1:g.21544del, NG_008098.1:g.21544dup, NG_008098.1:g.21543_21544dup, NG_008098.1:g.21542_21544dup, NG_008098.1:g.21541_21544dup, NG_008098.1:g.21540_21544dup, NG_008098.1:g.21539_21544dup, NG_008098.1:g.21538_21544dup, NG_008098.1:g.21537_21544dup, NG_008098.1:g.21536_21544dup, NG_008098.1:g.21535_21544dup, NG_008098.1:g.21534_21544dup, NG_008098.1:g.21533_21544dup, NG_008098.1:g.21530_21544dup, NG_008098.1:g.21528_21544dup, NG_008098.1:g.21527_21544dup, NG_008098.1:g.21544_21545insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

    2.

    rs1491463799 [Homo sapiens]
      Variant type:
      DELINS
      Alleles:
      ->AG,CG [Show Flanks]
      Chromosome:
      18:62385344 (GRCh38)
      18:60052578 (GRCh37)
      Canonical SPDI:
      NC_000018.10:62385344:G:GAG,NC_000018.10:62385344:G:GCG
      Gene:
      TNFRSF11A (Varview)
      Functional Consequence:
      3_prime_UTR_variant
      Validated:
      by frequency,by alfa,by cluster
      MAF:
      GAG=0.00051/6 (ALFA)
      GA=0.00219/141 (GnomAD)
      HGVS:
      NC_000018.10:g.62385345_62385346insAG, NC_000018.10:g.62385345_62385346insCG, NC_000018.9:g.60052578_60052579insAG, NC_000018.9:g.60052578_60052579insCG, NG_008098.1:g.65031_65032insAG, NG_008098.1:g.65031_65032insCG, NM_003839.4:c.*311_*312insAG, NM_003839.4:c.*311_*312insCG, NM_003839.3:c.*311_*312insAG, NM_003839.3:c.*311_*312insCG, NM_001278268.2:c.*311_*312insAG, NM_001278268.2:c.*311_*312insCG, NM_001278268.1:c.*311_*312insAG, NM_001278268.1:c.*311_*312insCG, NM_001270949.2:c.*586_*587insAG, NM_001270949.2:c.*586_*587insCG, NM_001270949.1:c.*586_*587insAG, NM_001270949.1:c.*586_*587insCG, NM_001270950.2:c.*311_*312insAG, NM_001270950.2:c.*311_*312insCG, NM_001270950.1:c.*311_*312insAG, NM_001270950.1:c.*311_*312insCG, NM_001270951.2:c.*311_*312insAG, NM_001270951.2:c.*311_*312insCG, NM_001270951.1:c.*311_*312insAG, NM_001270951.1:c.*311_*312insCG, XM_011526245.3:c.*311_*312insAG, XM_011526245.3:c.*311_*312insCG, XM_011526245.2:c.*311_*312insAG, XM_011526245.2:c.*311_*312insCG, XM_011526245.1:c.*311_*312insAG, XM_011526245.1:c.*311_*312insCG, XM_011526244.3:c.*311_*312insAG, XM_011526244.3:c.*311_*312insCG, XM_011526244.2:c.*311_*312insAG, XM_011526244.2:c.*311_*312insCG, XM_011526244.1:c.*311_*312insAG, XM_011526244.1:c.*311_*312insCG, XM_017026064.2:c.*311_*312insAG, XM_017026064.2:c.*311_*312insCG, XM_017026064.1:c.*311_*312insAG, XM_017026064.1:c.*311_*312insCG, XM_017026065.2:c.*311_*312insAG, XM_017026065.2:c.*311_*312insCG, XM_017026065.1:c.*311_*312insAG, XM_017026065.1:c.*311_*312insCG, XM_017026066.2:c.*311_*312insAG, XM_017026066.2:c.*311_*312insCG, XM_017026066.1:c.*311_*312insAG, XM_017026066.1:c.*311_*312insCG

      3.

      rs1491445691 [Homo sapiens]
        Variant type:
        DEL
        Alleles:
        CA>- [Show Flanks]
        Chromosome:
        18:62362490 (GRCh38)
        18:60029723 (GRCh37)
        Canonical SPDI:
        NC_000018.10:62362489:CA:
        Gene:
        TNFRSF11A (Varview)
        Functional Consequence:
        intron_variant
        Validated:
        by frequency,by alfa
        MAF:
        -=0.00059/7 (ALFA)
        HGVS:

        4.

        rs1491442279 [Homo sapiens]
          Variant type:
          DEL
          Alleles:
          CT>- [Show Flanks]
          Chromosome:
          18:62341836 (GRCh38)
          18:60009069 (GRCh37)
          Canonical SPDI:
          NC_000018.10:62341835:CT:
          Gene:
          TNFRSF11A (Varview)
          Functional Consequence:
          intron_variant,genic_upstream_transcript_variant
          Validated:
          by frequency,by alfa,by cluster
          MAF:
          -=0.00025/3 (ALFA)
          -=0.00004/1 (TOMMO)
          -=0.00077/49 (GnomAD)
          HGVS:

          5.

          rs1491414577 has merged into rs67721371 [Homo sapiens]
            Variant type:
            DELINS
            Alleles:
            TTTTTTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
            Chromosome:
            18:62367798 (GRCh38)
            18:60035031 (GRCh37)
            Canonical SPDI:
            NC_000018.10:62367788:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000018.10:62367788:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000018.10:62367788:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000018.10:62367788:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000018.10:62367788:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000018.10:62367788:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000018.10:62367788:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000018.10:62367788:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000018.10:62367788:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000018.10:62367788:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000018.10:62367788:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000018.10:62367788:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000018.10:62367788:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:62367788:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:62367788:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:62367788:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:62367788:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:62367788:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:62367788:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:62367788:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:62367788:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:62367788:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:62367788:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:62367788:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:62367788:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:62367788:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:62367788:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:62367788:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:62367788:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:62367788:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:62367788:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:62367788:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:62367788:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:62367788:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:62367788:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:62367788:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:62367788:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:62367788:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:62367788:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:62367788:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:62367788:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:62367788:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:62367788:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:62367788:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
            Gene:
            TNFRSF11A (Varview)
            Functional Consequence:
            intron_variant
            Validated:
            by frequency,by alfa,by cluster
            MAF:
            TTTTTTTTT=0./0 (ALFA)
            -=0.000004/1 (TOPMED)
            -=0.46885/2348 (1000Genomes)
            HGVS:
            NC_000018.10:g.62367798_62367811del, NC_000018.10:g.62367799_62367811del, NC_000018.10:g.62367800_62367811del, NC_000018.10:g.62367801_62367811del, NC_000018.10:g.62367802_62367811del, NC_000018.10:g.62367803_62367811del, NC_000018.10:g.62367805_62367811del, NC_000018.10:g.62367806_62367811del, NC_000018.10:g.62367807_62367811del, NC_000018.10:g.62367808_62367811del, NC_000018.10:g.62367809_62367811del, NC_000018.10:g.62367810_62367811del, NC_000018.10:g.62367811del, NC_000018.10:g.62367811dup, NC_000018.10:g.62367810_62367811dup, NC_000018.10:g.62367809_62367811dup, NC_000018.10:g.62367808_62367811dup, NC_000018.10:g.62367807_62367811dup, NC_000018.10:g.62367806_62367811dup, NC_000018.10:g.62367805_62367811dup, NC_000018.10:g.62367804_62367811dup, NC_000018.10:g.62367803_62367811dup, NC_000018.10:g.62367802_62367811dup, NC_000018.10:g.62367801_62367811dup, NC_000018.10:g.62367800_62367811dup, NC_000018.10:g.62367799_62367811dup, NC_000018.10:g.62367798_62367811dup, NC_000018.10:g.62367797_62367811dup, NC_000018.10:g.62367789_62367811T[38]CTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000018.10:g.62367796_62367811dup, NC_000018.10:g.62367795_62367811dup, NC_000018.10:g.62367794_62367811dup, NC_000018.10:g.62367793_62367811dup, NC_000018.10:g.62367792_62367811dup, NC_000018.10:g.62367791_62367811dup, NC_000018.10:g.62367790_62367811dup, NC_000018.10:g.62367789_62367811dup, NC_000018.10:g.62367811_62367812insTTTTTTTTTTTTTTTTTTTTTTTT, NC_000018.10:g.62367811_62367812insTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000018.10:g.62367811_62367812insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000018.10:g.62367811_62367812insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000018.10:g.62367811_62367812insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000018.10:g.62367811_62367812insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000018.10:g.62367811_62367812insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000018.9:g.60035031_60035044del, NC_000018.9:g.60035032_60035044del, NC_000018.9:g.60035033_60035044del, NC_000018.9:g.60035034_60035044del, NC_000018.9:g.60035035_60035044del, NC_000018.9:g.60035036_60035044del, NC_000018.9:g.60035038_60035044del, NC_000018.9:g.60035039_60035044del, NC_000018.9:g.60035040_60035044del, NC_000018.9:g.60035041_60035044del, NC_000018.9:g.60035042_60035044del, NC_000018.9:g.60035043_60035044del, NC_000018.9:g.60035044del, NC_000018.9:g.60035044dup, NC_000018.9:g.60035043_60035044dup, NC_000018.9:g.60035042_60035044dup, NC_000018.9:g.60035041_60035044dup, NC_000018.9:g.60035040_60035044dup, NC_000018.9:g.60035039_60035044dup, NC_000018.9:g.60035038_60035044dup, NC_000018.9:g.60035037_60035044dup, NC_000018.9:g.60035036_60035044dup, NC_000018.9:g.60035035_60035044dup, NC_000018.9:g.60035034_60035044dup, NC_000018.9:g.60035033_60035044dup, NC_000018.9:g.60035032_60035044dup, NC_000018.9:g.60035031_60035044dup, NC_000018.9:g.60035030_60035044dup, NC_000018.9:g.60035022_60035044T[38]CTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000018.9:g.60035029_60035044dup, NC_000018.9:g.60035028_60035044dup, NC_000018.9:g.60035027_60035044dup, NC_000018.9:g.60035026_60035044dup, NC_000018.9:g.60035025_60035044dup, NC_000018.9:g.60035024_60035044dup, NC_000018.9:g.60035023_60035044dup, NC_000018.9:g.60035022_60035044dup, NC_000018.9:g.60035044_60035045insTTTTTTTTTTTTTTTTTTTTTTTT, NC_000018.9:g.60035044_60035045insTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000018.9:g.60035044_60035045insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000018.9:g.60035044_60035045insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000018.9:g.60035044_60035045insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000018.9:g.60035044_60035045insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000018.9:g.60035044_60035045insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_008098.1:g.47484_47497del, NG_008098.1:g.47485_47497del, NG_008098.1:g.47486_47497del, NG_008098.1:g.47487_47497del, NG_008098.1:g.47488_47497del, NG_008098.1:g.47489_47497del, NG_008098.1:g.47491_47497del, NG_008098.1:g.47492_47497del, NG_008098.1:g.47493_47497del, NG_008098.1:g.47494_47497del, NG_008098.1:g.47495_47497del, NG_008098.1:g.47496_47497del, NG_008098.1:g.47497del, NG_008098.1:g.47497dup, NG_008098.1:g.47496_47497dup, NG_008098.1:g.47495_47497dup, NG_008098.1:g.47494_47497dup, NG_008098.1:g.47493_47497dup, NG_008098.1:g.47492_47497dup, NG_008098.1:g.47491_47497dup, NG_008098.1:g.47490_47497dup, NG_008098.1:g.47489_47497dup, NG_008098.1:g.47488_47497dup, NG_008098.1:g.47487_47497dup, NG_008098.1:g.47486_47497dup, NG_008098.1:g.47485_47497dup, NG_008098.1:g.47484_47497dup, NG_008098.1:g.47483_47497dup, NG_008098.1:g.47475_47497T[38]CTTTTTTTTTTTTTTTTTTTTTTTT[1], NG_008098.1:g.47482_47497dup, NG_008098.1:g.47481_47497dup, NG_008098.1:g.47480_47497dup, NG_008098.1:g.47479_47497dup, NG_008098.1:g.47478_47497dup, NG_008098.1:g.47477_47497dup, NG_008098.1:g.47476_47497dup, NG_008098.1:g.47475_47497dup, NG_008098.1:g.47497_47498insTTTTTTTTTTTTTTTTTTTTTTTT, NG_008098.1:g.47497_47498insTTTTTTTTTTTTTTTTTTTTTTTTT, NG_008098.1:g.47497_47498insTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_008098.1:g.47497_47498insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_008098.1:g.47497_47498insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_008098.1:g.47497_47498insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_008098.1:g.47497_47498insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

            6.

            rs1491410240 has merged into rs552069161 [Homo sapiens]
              Variant type:
              DELINS
              Alleles:
              GG>-,G,GGG,GGGG,GGGGG,GGGGGG [Show Flanks]
              Chromosome:
              18:62385353 (GRCh38)
              18:60052586 (GRCh37)
              Canonical SPDI:
              NC_000018.10:62385343:GGGGGGGGGGG:GGGGGGGGG,NC_000018.10:62385343:GGGGGGGGGGG:GGGGGGGGGG,NC_000018.10:62385343:GGGGGGGGGGG:GGGGGGGGGGGG,NC_000018.10:62385343:GGGGGGGGGGG:GGGGGGGGGGGGG,NC_000018.10:62385343:GGGGGGGGGGG:GGGGGGGGGGGGGG,NC_000018.10:62385343:GGGGGGGGGGG:GGGGGGGGGGGGGGG
              Gene:
              TNFRSF11A (Varview)
              Functional Consequence:
              3_prime_UTR_variant
              Clinical significance:
              uncertain-significance,likely-benign
              Validated:
              by frequency,by alfa,by cluster
              MAF:
              GGGGGGGGGGGGGG=0./0 (ALFA)
              -=0.15176/760 (1000Genomes)
              HGVS:
              NC_000018.10:g.62385353_62385354del, NC_000018.10:g.62385354del, NC_000018.10:g.62385354dup, NC_000018.10:g.62385353_62385354dup, NC_000018.10:g.62385352_62385354dup, NC_000018.10:g.62385351_62385354dup, NC_000018.9:g.60052586_60052587del, NC_000018.9:g.60052587del, NC_000018.9:g.60052587dup, NC_000018.9:g.60052586_60052587dup, NC_000018.9:g.60052585_60052587dup, NC_000018.9:g.60052584_60052587dup, NG_008098.1:g.65039_65040del, NG_008098.1:g.65040del, NG_008098.1:g.65040dup, NG_008098.1:g.65039_65040dup, NG_008098.1:g.65038_65040dup, NG_008098.1:g.65037_65040dup, NM_003839.4:c.*319_*320del, NM_003839.4:c.*320del, NM_003839.4:c.*320dup, NM_003839.4:c.*319_*320dup, NM_003839.4:c.*318_*320dup, NM_003839.4:c.*317_*320dup, NM_003839.3:c.*319_*320del, NM_003839.3:c.*320del, NM_003839.3:c.*320dup, NM_003839.3:c.*319_*320dup, NM_003839.3:c.*318_*320dup, NM_003839.3:c.*317_*320dup, NM_001278268.2:c.*319_*320del, NM_001278268.2:c.*320del, NM_001278268.2:c.*320dup, NM_001278268.2:c.*319_*320dup, NM_001278268.2:c.*318_*320dup, NM_001278268.2:c.*317_*320dup, NM_001278268.1:c.*319_*320del, NM_001278268.1:c.*320del, NM_001278268.1:c.*320dup, NM_001278268.1:c.*319_*320dup, NM_001278268.1:c.*318_*320dup, NM_001278268.1:c.*317_*320dup, NM_001270949.2:c.*594_*595del, NM_001270949.2:c.*595del, NM_001270949.2:c.*595dup, NM_001270949.2:c.*594_*595dup, NM_001270949.2:c.*593_*595dup, NM_001270949.2:c.*592_*595dup, NM_001270949.1:c.*594_*595del, NM_001270949.1:c.*595del, NM_001270949.1:c.*595dup, NM_001270949.1:c.*594_*595dup, NM_001270949.1:c.*593_*595dup, NM_001270949.1:c.*592_*595dup, NM_001270950.2:c.*319_*320del, NM_001270950.2:c.*320del, NM_001270950.2:c.*320dup, NM_001270950.2:c.*319_*320dup, NM_001270950.2:c.*318_*320dup, NM_001270950.2:c.*317_*320dup, NM_001270950.1:c.*319_*320del, NM_001270950.1:c.*320del, NM_001270950.1:c.*320dup, NM_001270950.1:c.*319_*320dup, NM_001270950.1:c.*318_*320dup, NM_001270950.1:c.*317_*320dup, NM_001270951.2:c.*319_*320del, NM_001270951.2:c.*320del, NM_001270951.2:c.*320dup, NM_001270951.2:c.*319_*320dup, NM_001270951.2:c.*318_*320dup, NM_001270951.2:c.*317_*320dup, NM_001270951.1:c.*319_*320del, NM_001270951.1:c.*320del, NM_001270951.1:c.*320dup, NM_001270951.1:c.*319_*320dup, NM_001270951.1:c.*318_*320dup, NM_001270951.1:c.*317_*320dup, XM_011526245.3:c.*319_*320del, XM_011526245.3:c.*320del, XM_011526245.3:c.*320dup, XM_011526245.3:c.*319_*320dup, XM_011526245.3:c.*318_*320dup, XM_011526245.3:c.*317_*320dup, XM_011526245.2:c.*319_*320del, XM_011526245.2:c.*320del, XM_011526245.2:c.*320dup, XM_011526245.2:c.*319_*320dup, XM_011526245.2:c.*318_*320dup, XM_011526245.2:c.*317_*320dup, XM_011526245.1:c.*319_*320del, XM_011526245.1:c.*320del, XM_011526245.1:c.*320dup, XM_011526245.1:c.*319_*320dup, XM_011526245.1:c.*318_*320dup, XM_011526245.1:c.*317_*320dup, XM_011526244.3:c.*319_*320del, XM_011526244.3:c.*320del, XM_011526244.3:c.*320dup, XM_011526244.3:c.*319_*320dup, XM_011526244.3:c.*318_*320dup, XM_011526244.3:c.*317_*320dup, XM_011526244.2:c.*319_*320del, XM_011526244.2:c.*320del, XM_011526244.2:c.*320dup, XM_011526244.2:c.*319_*320dup, XM_011526244.2:c.*318_*320dup, XM_011526244.2:c.*317_*320dup, XM_011526244.1:c.*319_*320del, XM_011526244.1:c.*320del, XM_011526244.1:c.*320dup, XM_011526244.1:c.*319_*320dup, XM_011526244.1:c.*318_*320dup, XM_011526244.1:c.*317_*320dup, XM_017026064.2:c.*319_*320del, XM_017026064.2:c.*320del, XM_017026064.2:c.*320dup, XM_017026064.2:c.*319_*320dup, XM_017026064.2:c.*318_*320dup, XM_017026064.2:c.*317_*320dup, XM_017026064.1:c.*319_*320del, XM_017026064.1:c.*320del, XM_017026064.1:c.*320dup, XM_017026064.1:c.*319_*320dup, XM_017026064.1:c.*318_*320dup, XM_017026064.1:c.*317_*320dup, XM_017026065.2:c.*319_*320del, XM_017026065.2:c.*320del, XM_017026065.2:c.*320dup, XM_017026065.2:c.*319_*320dup, XM_017026065.2:c.*318_*320dup, XM_017026065.2:c.*317_*320dup, XM_017026065.1:c.*319_*320del, XM_017026065.1:c.*320del, XM_017026065.1:c.*320dup, XM_017026065.1:c.*319_*320dup, XM_017026065.1:c.*318_*320dup, XM_017026065.1:c.*317_*320dup, XM_017026066.2:c.*319_*320del, XM_017026066.2:c.*320del, XM_017026066.2:c.*320dup, XM_017026066.2:c.*319_*320dup, XM_017026066.2:c.*318_*320dup, XM_017026066.2:c.*317_*320dup, XM_017026066.1:c.*319_*320del, XM_017026066.1:c.*320del, XM_017026066.1:c.*320dup, XM_017026066.1:c.*319_*320dup, XM_017026066.1:c.*318_*320dup, XM_017026066.1:c.*317_*320dup

              7.

              rs1491387782 [Homo sapiens]
                Variant type:
                DELINS
                Alleles:
                ->CT [Show Flanks]
                Chromosome:
                18:62367789 (GRCh38)
                18:60035023 (GRCh37)
                Canonical SPDI:
                NC_000018.10:62367789:T:TCT
                Gene:
                TNFRSF11A (Varview)
                Functional Consequence:
                intron_variant
                Validated:
                by frequency,by alfa
                MAF:
                TCT=0./0 (ALFA)
                HGVS:

                8.

                rs1491374525 [Homo sapiens]
                  Variant type:
                  SNV:
                  Alleles:
                  ->TTTA
                  Chromosome:
                  no mapping
                  Canonical SPDI:

                  9.

                  rs1491294842 [Homo sapiens]
                    Variant type:
                    DELINS
                    Alleles:
                    ->G,GG [Show Flanks]
                    Chromosome:
                    18:62337018 (GRCh38)
                    18:60004252 (GRCh37)
                    Canonical SPDI:
                    NC_000018.10:62337018:G:GG,NC_000018.10:62337018:G:GGG
                    Gene:
                    TNFRSF11A (Varview)
                    Functional Consequence:
                    intron_variant,genic_upstream_transcript_variant
                    Validated:
                    by frequency,by alfa,by cluster
                    MAF:
                    GG=0./0 (ALFA)
                    G=0.000181/48 (TOPMED)
                    G=0.000223/1 (Estonian)
                    G=0.000309/43 (GnomAD)
                    G=0.001638/3 (Korea1K)
                    HGVS:

                    10.

                    rs1491263419 [Homo sapiens]
                      Variant type:
                      DEL
                      Alleles:
                      TG>- [Show Flanks]
                      Chromosome:
                      18:62363386 (GRCh38)
                      18:60030619 (GRCh37)
                      Canonical SPDI:
                      NC_000018.10:62363385:TG:
                      Gene:
                      TNFRSF11A (Varview)
                      Functional Consequence:
                      intron_variant
                      Validated:
                      by frequency,by alfa,by cluster
                      MAF:
                      -=0.048643/577 (ALFA)
                      -=0.003197/337 (GnomAD)
                      -=0.011001/20 (Korea1K)
                      -=0.013454/225 (TOMMO)
                      HGVS:

                      11.

                      rs1491259500 [Homo sapiens]
                        Variant type:
                        DEL
                        Alleles:
                        CA>- [Show Flanks]
                        Chromosome:
                        18:62342401 (GRCh38)
                        18:60009634 (GRCh37)
                        Canonical SPDI:
                        NC_000018.10:62342400:CA:
                        Gene:
                        TNFRSF11A (Varview)
                        Functional Consequence:
                        intron_variant,genic_upstream_transcript_variant
                        Validated:
                        by frequency,by alfa
                        MAF:
                        -=0.00261/31 (ALFA)
                        HGVS:

                        12.

                        rs1491253159 [Homo sapiens]
                          Variant type:
                          INS
                          Alleles:
                          ->C [Show Flanks]
                          Chromosome:
                          18:62341837 (GRCh38)
                          18:60009071 (GRCh37)
                          Canonical SPDI:
                          NC_000018.10:62341837::C
                          Gene:
                          TNFRSF11A (Varview)
                          Functional Consequence:
                          intron_variant,genic_upstream_transcript_variant
                          Validated:
                          by frequency,by alfa
                          MAF:
                          C=0./0 (ALFA)
                          C=0.00022/1 (GnomAD)
                          HGVS:

                          13.

                          rs1491176958 [Homo sapiens]
                            Variant type:
                            DELINS
                            Alleles:
                            ->CTTT [Show Flanks]
                            Chromosome:
                            18:62370836 (GRCh38)
                            18:60038070 (GRCh37)
                            Canonical SPDI:
                            NC_000018.10:62370836:TTT:TTTCTTT
                            Gene:
                            TNFRSF11A (Varview)
                            Functional Consequence:
                            intron_variant
                            Validated:
                            by frequency,by alfa,by cluster
                            MAF:
                            TTTCTTT=0.00008/1 (ALFA)
                            TTTC=0.00446/10 (GnomAD)
                            HGVS:

                            14.

                            rs1491033265 has merged into rs71160826 [Homo sapiens]
                              Variant type:
                              DELINS
                              Alleles:
                              TTTTTTTT>-,T,TTTTT,TTTTTT,TTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
                              Chromosome:
                              18:62351013 (GRCh38)
                              18:60018246 (GRCh37)
                              Canonical SPDI:
                              NC_000018.10:62351002:TTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000018.10:62351002:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000018.10:62351002:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000018.10:62351002:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000018.10:62351002:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000018.10:62351002:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000018.10:62351002:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000018.10:62351002:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000018.10:62351002:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:62351002:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:62351002:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:62351002:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:62351002:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:62351002:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:62351002:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:62351002:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:62351002:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:62351002:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:62351002:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:62351002:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:62351002:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:62351002:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
                              Gene:
                              TNFRSF11A (Varview)
                              Functional Consequence:
                              intron_variant
                              Validated:
                              by frequency,by alfa,by cluster
                              MAF:
                              TTTTTTTTTTTTTTTT=0./0 (ALFA)
                              -=0.26757/1340 (1000Genomes)
                              HGVS:
                              NC_000018.10:g.62351013_62351020del, NC_000018.10:g.62351014_62351020del, NC_000018.10:g.62351018_62351020del, NC_000018.10:g.62351019_62351020del, NC_000018.10:g.62351020del, NC_000018.10:g.62351020dup, NC_000018.10:g.62351019_62351020dup, NC_000018.10:g.62351018_62351020dup, NC_000018.10:g.62351017_62351020dup, NC_000018.10:g.62351016_62351020dup, NC_000018.10:g.62351015_62351020dup, NC_000018.10:g.62351014_62351020dup, NC_000018.10:g.62351013_62351020dup, NC_000018.10:g.62351011_62351020dup, NC_000018.10:g.62351010_62351020dup, NC_000018.10:g.62351009_62351020dup, NC_000018.10:g.62351008_62351020dup, NC_000018.10:g.62351007_62351020dup, NC_000018.10:g.62351006_62351020dup, NC_000018.10:g.62351020_62351021insTTTTTTTTTTTTTTTTTTTTT, NC_000018.10:g.62351020_62351021insTTTTTTTTTTTTTTTTTTTTTTT, NC_000018.10:g.62351020_62351021insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000018.9:g.60018246_60018253del, NC_000018.9:g.60018247_60018253del, NC_000018.9:g.60018251_60018253del, NC_000018.9:g.60018252_60018253del, NC_000018.9:g.60018253del, NC_000018.9:g.60018253dup, NC_000018.9:g.60018252_60018253dup, NC_000018.9:g.60018251_60018253dup, NC_000018.9:g.60018250_60018253dup, NC_000018.9:g.60018249_60018253dup, NC_000018.9:g.60018248_60018253dup, NC_000018.9:g.60018247_60018253dup, NC_000018.9:g.60018246_60018253dup, NC_000018.9:g.60018244_60018253dup, NC_000018.9:g.60018243_60018253dup, NC_000018.9:g.60018242_60018253dup, NC_000018.9:g.60018241_60018253dup, NC_000018.9:g.60018240_60018253dup, NC_000018.9:g.60018239_60018253dup, NC_000018.9:g.60018253_60018254insTTTTTTTTTTTTTTTTTTTTT, NC_000018.9:g.60018253_60018254insTTTTTTTTTTTTTTTTTTTTTTT, NC_000018.9:g.60018253_60018254insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_008098.1:g.30699_30706del, NG_008098.1:g.30700_30706del, NG_008098.1:g.30704_30706del, NG_008098.1:g.30705_30706del, NG_008098.1:g.30706del, NG_008098.1:g.30706dup, NG_008098.1:g.30705_30706dup, NG_008098.1:g.30704_30706dup, NG_008098.1:g.30703_30706dup, NG_008098.1:g.30702_30706dup, NG_008098.1:g.30701_30706dup, NG_008098.1:g.30700_30706dup, NG_008098.1:g.30699_30706dup, NG_008098.1:g.30697_30706dup, NG_008098.1:g.30696_30706dup, NG_008098.1:g.30695_30706dup, NG_008098.1:g.30694_30706dup, NG_008098.1:g.30693_30706dup, NG_008098.1:g.30692_30706dup, NG_008098.1:g.30706_30707insTTTTTTTTTTTTTTTTTTTTT, NG_008098.1:g.30706_30707insTTTTTTTTTTTTTTTTTTTTTTT, NG_008098.1:g.30706_30707insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

                              15.

                              rs1491017571 [Homo sapiens]
                                Variant type:
                                DELINS
                                Alleles:
                                ->AAAAAAAAAAAAAAAAACA,AAAAAAAAACA,AAAAAAACA [Show Flanks]
                                Chromosome:
                                18:62342424 (GRCh38)
                                18:60009658 (GRCh37)
                                Canonical SPDI:
                                NC_000018.10:62342424:A:AAAAAAAAAAAAAAAAAACA,NC_000018.10:62342424:A:AAAAAAAAAACA,NC_000018.10:62342424:A:AAAAAAAACA
                                Gene:
                                TNFRSF11A (Varview)
                                Functional Consequence:
                                intron_variant,genic_upstream_transcript_variant
                                Validated:
                                by frequency,by alfa
                                MAF:
                                AAAAAAAAAACA=0.00006/1 (ALFA)
                                HGVS:

                                16.

                                rs1490993841 [Homo sapiens]
                                  Variant type:
                                  SNV
                                  Alleles:
                                  G>C [Show Flanks]
                                  Chromosome:
                                  18:62364888 (GRCh38)
                                  18:60032121 (GRCh37)
                                  Canonical SPDI:
                                  NC_000018.10:62364887:G:C
                                  Gene:
                                  TNFRSF11A (Varview)
                                  Functional Consequence:
                                  intron_variant
                                  Validated:
                                  by frequency,by alfa
                                  MAF:
                                  C=0./0 (ALFA)
                                  C=0.000008/2 (TOPMED)
                                  HGVS:

                                  17.

                                  rs1490925609 [Homo sapiens]
                                    Variant type:
                                    DELINS
                                    Alleles:
                                    ->T [Show Flanks]
                                    Chromosome:
                                    18:62349181 (GRCh38)
                                    18:60016415 (GRCh37)
                                    Canonical SPDI:
                                    NC_000018.10:62349181:TTTTTTT:TTTTTTTT
                                    Gene:
                                    TNFRSF11A (Varview)
                                    Functional Consequence:
                                    intron_variant
                                    Validated:
                                    by frequency,by alfa
                                    MAF:
                                    TTTTTTTT=0.000084/1 (ALFA)
                                    T=0.000036/4 (GnomAD)
                                    HGVS:

                                    18.

                                    rs1490876099 [Homo sapiens]
                                      Variant type:
                                      SNV
                                      Alleles:
                                      T>G [Show Flanks]
                                      Chromosome:
                                      18:62348882 (GRCh38)
                                      18:60016115 (GRCh37)
                                      Canonical SPDI:
                                      NC_000018.10:62348881:T:G
                                      Gene:
                                      TNFRSF11A (Varview)
                                      Functional Consequence:
                                      intron_variant
                                      Validated:
                                      by frequency,by alfa,by cluster
                                      MAF:
                                      G=0.000071/1 (ALFA)
                                      G=0.000004/1 (TOPMED)
                                      G=0.000014/2 (GnomAD)
                                      HGVS:

                                      19.

                                      rs1490872827 [Homo sapiens]
                                        Variant type:
                                        SNV
                                        Alleles:
                                        T>C [Show Flanks]
                                        Chromosome:
                                        18:62382178 (GRCh38)
                                        18:60049411 (GRCh37)
                                        Canonical SPDI:
                                        NC_000018.10:62382177:T:C
                                        Gene:
                                        TNFRSF11A (Varview)
                                        Functional Consequence:
                                        intron_variant
                                        Validated:
                                        by frequency,by alfa,by cluster
                                        MAF:
                                        C=0.000071/1 (ALFA)
                                        C=0.000004/1 (TOPMED)
                                        C=0.000015/2 (GnomAD)
                                        HGVS:

                                        20.

                                        rs1490790576 [Homo sapiens]
                                          Variant type:
                                          SNV
                                          Alleles:
                                          T>C [Show Flanks]
                                          Chromosome:
                                          18:62372705 (GRCh38)
                                          18:60039938 (GRCh37)
                                          Canonical SPDI:
                                          NC_000018.10:62372704:T:C
                                          Gene:
                                          TNFRSF11A (Varview)
                                          Functional Consequence:
                                          intron_variant
                                          Validated:
                                          by frequency,by alfa,by cluster
                                          MAF:
                                          C=0./0 (ALFA)
                                          C=0.000004/1 (TOPMED)
                                          C=0.000007/1 (GnomAD)
                                          HGVS:

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