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Items: 1 to 20 of 524

1.

rs1490924575 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    T>G [Show Flanks]
    Chromosome:
    5:143400282 (GRCh38)
    5:142779847 (GRCh37)
    Canonical SPDI:
    NC_000005.10:143400281:T:G
    Gene:
    NR3C1 (Varview)
    Functional Consequence:
    5_prime_UTR_variant,intron_variant,synonymous_variant,coding_sequence_variant
    HGVS:
    NC_000005.10:g.143400282T>G, NC_000005.9:g.142779847T>G, NG_009062.1:g.40231A>C, NM_000176.3:c.558A>C, NM_000176.2:c.558A>C, NM_001024094.2:c.558A>C, NM_001024094.1:c.558A>C, NM_001204264.2:c.-448A>C, NM_001204264.1:c.-448A>C, NM_001204263.2:c.-433A>C, NM_001204263.1:c.-433A>C, NM_001204262.2:c.-388A>C, NM_001204262.1:c.-388A>C, NM_001204261.2:c.267A>C, NM_001204261.1:c.267A>C, NM_001204260.2:c.291A>C, NM_001204260.1:c.291A>C, NM_001204259.2:c.303A>C, NM_001204259.1:c.303A>C, NM_001204258.2:c.480A>C, NM_001204258.1:c.480A>C, NM_001364183.2:c.558A>C, NM_001364183.1:c.558A>C, NM_001364181.2:c.558A>C, NM_001364181.1:c.558A>C, NM_001364180.2:c.558A>C, NM_001364180.1:c.558A>C, NM_001364184.2:c.558A>C, NM_001364184.1:c.558A>C, NM_001018076.2:c.558A>C, NM_001018076.1:c.558A>C, NM_001020825.2:c.558A>C, NM_001020825.1:c.558A>C, NM_001204265.2:c.558A>C, NM_001204265.1:c.558A>C, NM_001018077.1:c.558A>C, NM_001364185.1:c.558A>C, NM_001364182.1:c.558A>C, NM_001018074.1:c.558A>C, NM_001018075.1:c.558A>C

    2.

    rs1490798691 [Homo sapiens]
      Variant type:
      SNV
      Alleles:
      T>C [Show Flanks]
      Chromosome:
      5:143310128 (GRCh38)
      5:142689693 (GRCh37)
      Canonical SPDI:
      NC_000005.10:143310127:T:C
      Gene:
      NR3C1 (Varview)
      Functional Consequence:
      synonymous_variant,non_coding_transcript_variant,coding_sequence_variant
      Validated:
      by frequency,by alfa
      MAF:
      C=0.000084/1 (ALFA)
      C=0.000004/1 (TOPMED)
      HGVS:
      NC_000005.10:g.143310128T>C, NC_000005.9:g.142689693T>C, NG_009062.1:g.130385A>G, NM_000176.3:c.1437A>G, NM_000176.2:c.1437A>G, NM_001024094.2:c.1440A>G, NM_001024094.1:c.1440A>G, NM_001204264.2:c.432A>G, NM_001204264.1:c.432A>G, NM_001204263.2:c.447A>G, NM_001204263.1:c.447A>G, NM_001204262.2:c.492A>G, NM_001204262.1:c.492A>G, NM_001204261.2:c.1146A>G, NM_001204261.1:c.1146A>G, NM_001204260.2:c.1170A>G, NM_001204260.1:c.1170A>G, NM_001204259.2:c.1182A>G, NM_001204259.1:c.1182A>G, NM_001204258.2:c.1359A>G, NM_001204258.1:c.1359A>G, NM_001364183.2:c.1440A>G, NM_001364183.1:c.1440A>G, NM_001364181.2:c.1437A>G, NM_001364181.1:c.1437A>G, NM_001364180.2:c.1437A>G, NM_001364180.1:c.1437A>G, NM_001364184.2:c.1440A>G, NM_001364184.1:c.1440A>G, NM_001018076.2:c.1437A>G, NM_001018076.1:c.1437A>G, NR_157096.2:n.360A>G, NR_157096.1:n.360A>G, NM_001020825.2:c.1437A>G, NM_001020825.1:c.1437A>G, NM_001204265.2:c.1437A>G, NM_001204265.1:c.1437A>G, NM_001018077.1:c.1437A>G, NM_001364185.1:c.1440A>G, NM_001364182.1:c.1437A>G, NM_001018074.1:c.1437A>G, NM_001018075.1:c.1437A>G

      3.

      rs1490656320 [Homo sapiens]
        Variant type:
        SNV
        Alleles:
        T>C,G [Show Flanks]
        Chromosome:
        5:143399928 (GRCh38)
        5:142779493 (GRCh37)
        Canonical SPDI:
        NC_000005.10:143399927:T:C,NC_000005.10:143399927:T:G
        Gene:
        NR3C1 (Varview)
        Functional Consequence:
        5_prime_UTR_variant,intron_variant,synonymous_variant,coding_sequence_variant
        Validated:
        by frequency,by alfa
        MAF:
        G=0./0 (ALFA)
        HGVS:
        NC_000005.10:g.143399928T>C, NC_000005.10:g.143399928T>G, NC_000005.9:g.142779493T>C, NC_000005.9:g.142779493T>G, NG_009062.1:g.40585A>G, NG_009062.1:g.40585A>C, NM_000176.3:c.912A>G, NM_000176.3:c.912A>C, NM_000176.2:c.912A>G, NM_000176.2:c.912A>C, NM_001024094.2:c.912A>G, NM_001024094.2:c.912A>C, NM_001024094.1:c.912A>G, NM_001024094.1:c.912A>C, NM_001204264.2:c.-94A>G, NM_001204264.2:c.-94A>C, NM_001204264.1:c.-94A>G, NM_001204264.1:c.-94A>C, NM_001204263.2:c.-79A>G, NM_001204263.2:c.-79A>C, NM_001204263.1:c.-79A>G, NM_001204263.1:c.-79A>C, NM_001204262.2:c.-34A>G, NM_001204262.2:c.-34A>C, NM_001204262.1:c.-34A>G, NM_001204262.1:c.-34A>C, NM_001204261.2:c.621A>G, NM_001204261.2:c.621A>C, NM_001204261.1:c.621A>G, NM_001204261.1:c.621A>C, NM_001204260.2:c.645A>G, NM_001204260.2:c.645A>C, NM_001204260.1:c.645A>G, NM_001204260.1:c.645A>C, NM_001204259.2:c.657A>G, NM_001204259.2:c.657A>C, NM_001204259.1:c.657A>G, NM_001204259.1:c.657A>C, NM_001204258.2:c.834A>G, NM_001204258.2:c.834A>C, NM_001204258.1:c.834A>G, NM_001204258.1:c.834A>C, NM_001364183.2:c.912A>G, NM_001364183.2:c.912A>C, NM_001364183.1:c.912A>G, NM_001364183.1:c.912A>C, NM_001364181.2:c.912A>G, NM_001364181.2:c.912A>C, NM_001364181.1:c.912A>G, NM_001364181.1:c.912A>C, NM_001364180.2:c.912A>G, NM_001364180.2:c.912A>C, NM_001364180.1:c.912A>G, NM_001364180.1:c.912A>C, NM_001364184.2:c.912A>G, NM_001364184.2:c.912A>C, NM_001364184.1:c.912A>G, NM_001364184.1:c.912A>C, NM_001018076.2:c.912A>G, NM_001018076.2:c.912A>C, NM_001018076.1:c.912A>G, NM_001018076.1:c.912A>C, NM_001020825.2:c.912A>G, NM_001020825.2:c.912A>C, NM_001020825.1:c.912A>G, NM_001020825.1:c.912A>C, NM_001204265.2:c.912A>G, NM_001204265.2:c.912A>C, NM_001204265.1:c.912A>G, NM_001204265.1:c.912A>C, NM_001018077.1:c.912A>G, NM_001018077.1:c.912A>C, NM_001364185.1:c.912A>G, NM_001364185.1:c.912A>C, NM_001364182.1:c.912A>G, NM_001364182.1:c.912A>C, NM_001018074.1:c.912A>G, NM_001018074.1:c.912A>C, NM_001018075.1:c.912A>G, NM_001018075.1:c.912A>C

        4.

        rs1489765141 [Homo sapiens]
          Variant type:
          SNV
          Alleles:
          T>C [Show Flanks]
          Chromosome:
          5:143399967 (GRCh38)
          5:142779532 (GRCh37)
          Canonical SPDI:
          NC_000005.10:143399966:T:C
          Gene:
          NR3C1 (Varview)
          Functional Consequence:
          5_prime_UTR_variant,intron_variant,synonymous_variant,coding_sequence_variant
          Validated:
          by frequency
          MAF:
          C=0.000004/1 (GnomAD_exomes)
          HGVS:
          NC_000005.10:g.143399967T>C, NC_000005.9:g.142779532T>C, NG_009062.1:g.40546A>G, NM_000176.3:c.873A>G, NM_000176.2:c.873A>G, NM_001024094.2:c.873A>G, NM_001024094.1:c.873A>G, NM_001204264.2:c.-133A>G, NM_001204264.1:c.-133A>G, NM_001204263.2:c.-118A>G, NM_001204263.1:c.-118A>G, NM_001204262.2:c.-73A>G, NM_001204262.1:c.-73A>G, NM_001204261.2:c.582A>G, NM_001204261.1:c.582A>G, NM_001204260.2:c.606A>G, NM_001204260.1:c.606A>G, NM_001204259.2:c.618A>G, NM_001204259.1:c.618A>G, NM_001204258.2:c.795A>G, NM_001204258.1:c.795A>G, NM_001364183.2:c.873A>G, NM_001364183.1:c.873A>G, NM_001364181.2:c.873A>G, NM_001364181.1:c.873A>G, NM_001364180.2:c.873A>G, NM_001364180.1:c.873A>G, NM_001364184.2:c.873A>G, NM_001364184.1:c.873A>G, NM_001018076.2:c.873A>G, NM_001018076.1:c.873A>G, NM_001020825.2:c.873A>G, NM_001020825.1:c.873A>G, NM_001204265.2:c.873A>G, NM_001204265.1:c.873A>G, NM_001018077.1:c.873A>G, NM_001364185.1:c.873A>G, NM_001364182.1:c.873A>G, NM_001018074.1:c.873A>G, NM_001018075.1:c.873A>G

          5.

          rs1486156457 [Homo sapiens]
            Variant type:
            SNV
            Alleles:
            G>A [Show Flanks]
            Chromosome:
            5:143281949 (GRCh38)
            5:142661514 (GRCh37)
            Canonical SPDI:
            NC_000005.10:143281948:G:A
            Gene:
            NR3C1 (Varview)
            Functional Consequence:
            intron_variant,synonymous_variant,coding_sequence_variant,non_coding_transcript_variant,genic_downstream_transcript_variant
            Validated:
            by frequency,by alfa
            MAF:
            A=0./0 (ALFA)
            HGVS:
            NC_000005.10:g.143281949G>A, NC_000005.9:g.142661514G>A, NG_009062.1:g.158564C>T, NM_000176.3:c.2274C>T, NM_000176.2:c.2274C>T, NM_001024094.2:c.2277C>T, NM_001024094.1:c.2277C>T, NM_001204264.2:c.1269C>T, NM_001204264.1:c.1269C>T, NM_001204263.2:c.1284C>T, NM_001204263.1:c.1284C>T, NM_001204262.2:c.1329C>T, NM_001204262.1:c.1329C>T, NM_001204261.2:c.1983C>T, NM_001204261.1:c.1983C>T, NM_001204260.2:c.2007C>T, NM_001204260.1:c.2007C>T, NM_001204259.2:c.2019C>T, NM_001204259.1:c.2019C>T, NM_001204258.2:c.2196C>T, NM_001204258.1:c.2196C>T, NM_001364183.2:c.2277C>T, NM_001364183.1:c.2277C>T, NM_001364181.2:c.2274C>T, NM_001364181.1:c.2274C>T, NM_001364180.2:c.2274C>T, NM_001364180.1:c.2274C>T, NM_001364184.2:c.2277C>T, NM_001364184.1:c.2277C>T, NM_001018076.2:c.2274C>T, NM_001018076.1:c.2274C>T, NR_157096.2:n.1197C>T, NR_157096.1:n.1197C>T, NM_001018077.1:c.2274C>T, NM_001364185.1:c.2277C>T, NM_001364182.1:c.2274C>T, NM_001018074.1:c.2274C>T, NM_001018075.1:c.2274C>T

            6.

            rs1486098461 [Homo sapiens]
              Variant type:
              SNV
              Alleles:
              G>C [Show Flanks]
              Chromosome:
              5:143400515 (GRCh38)
              5:142780080 (GRCh37)
              Canonical SPDI:
              NC_000005.10:143400514:G:C
              Gene:
              NR3C1 (Varview)
              Functional Consequence:
              5_prime_UTR_variant,intron_variant,missense_variant,coding_sequence_variant
              Validated:
              by frequency,by alfa,by cluster
              MAF:
              C=0.000028/1 (ALFA)
              C=0.000004/1 (GnomAD_exomes)
              C=0.000004/1 (TOPMED)
              HGVS:
              NC_000005.10:g.143400515G>C, NC_000005.9:g.142780080G>C, NG_009062.1:g.39998C>G, NM_000176.3:c.325C>G, NM_000176.2:c.325C>G, NM_001024094.2:c.325C>G, NM_001024094.1:c.325C>G, NM_001204264.2:c.-681C>G, NM_001204264.1:c.-681C>G, NM_001204263.2:c.-666C>G, NM_001204263.1:c.-666C>G, NM_001204262.2:c.-621C>G, NM_001204262.1:c.-621C>G, NM_001204261.2:c.34C>G, NM_001204261.1:c.34C>G, NM_001204260.2:c.58C>G, NM_001204260.1:c.58C>G, NM_001204259.2:c.70C>G, NM_001204259.1:c.70C>G, NM_001204258.2:c.247C>G, NM_001204258.1:c.247C>G, NM_001364183.2:c.325C>G, NM_001364183.1:c.325C>G, NM_001364181.2:c.325C>G, NM_001364181.1:c.325C>G, NM_001364180.2:c.325C>G, NM_001364180.1:c.325C>G, NM_001364184.2:c.325C>G, NM_001364184.1:c.325C>G, NM_001018076.2:c.325C>G, NM_001018076.1:c.325C>G, NM_001020825.2:c.325C>G, NM_001020825.1:c.325C>G, NM_001204265.2:c.325C>G, NM_001204265.1:c.325C>G, NM_001018077.1:c.325C>G, NM_001364185.1:c.325C>G, NM_001364182.1:c.325C>G, NM_001018074.1:c.325C>G, NM_001018075.1:c.325C>G, NP_000167.1:p.Gln109Glu, NP_001019265.1:p.Gln109Glu, NP_001191190.1:p.Gln12Glu, NP_001191189.1:p.Gln20Glu, NP_001191188.1:p.Gln24Glu, NP_001191187.1:p.Gln83Glu, NP_001351112.1:p.Gln109Glu, NP_001351110.1:p.Gln109Glu, NP_001351109.1:p.Gln109Glu, NP_001351113.1:p.Gln109Glu, NP_001018086.1:p.Gln109Glu, NP_001018661.1:p.Gln109Glu, NP_001191194.1:p.Gln109Glu, NP_001018087.1:p.Gln109Glu, NP_001351114.1:p.Gln109Glu, NP_001351111.1:p.Gln109Glu, NP_001018084.1:p.Gln109Glu, NP_001018085.1:p.Gln109Glu

              7.

              rs1483819721 [Homo sapiens]
                Variant type:
                SNV
                Alleles:
                T>G [Show Flanks]
                Chromosome:
                5:143282652 (GRCh38)
                5:142662217 (GRCh37)
                Canonical SPDI:
                NC_000005.10:143282651:T:G
                Gene:
                NR3C1 (Varview)
                Functional Consequence:
                non_coding_transcript_variant,missense_variant,genic_downstream_transcript_variant,coding_sequence_variant
                Validated:
                by frequency
                MAF:
                G=0.000008/2 (GnomAD_exomes)
                HGVS:
                NC_000005.10:g.143282652T>G, NC_000005.9:g.142662217T>G, NG_009062.1:g.157861A>C, NM_000176.3:c.2097A>C, NM_000176.2:c.2097A>C, NM_001024094.2:c.2100A>C, NM_001024094.1:c.2100A>C, NM_001204264.2:c.1092A>C, NM_001204264.1:c.1092A>C, NM_001204263.2:c.1107A>C, NM_001204263.1:c.1107A>C, NM_001204262.2:c.1152A>C, NM_001204262.1:c.1152A>C, NM_001204261.2:c.1806A>C, NM_001204261.1:c.1806A>C, NM_001204260.2:c.1830A>C, NM_001204260.1:c.1830A>C, NM_001204259.2:c.1842A>C, NM_001204259.1:c.1842A>C, NM_001204258.2:c.2019A>C, NM_001204258.1:c.2019A>C, NM_001364183.2:c.2100A>C, NM_001364183.1:c.2100A>C, NM_001364181.2:c.2097A>C, NM_001364181.1:c.2097A>C, NM_001364180.2:c.2097A>C, NM_001364180.1:c.2097A>C, NM_001364184.2:c.2100A>C, NM_001364184.1:c.2100A>C, NM_001018076.2:c.2097A>C, NM_001018076.1:c.2097A>C, NR_157096.2:n.1020A>C, NR_157096.1:n.1020A>C, NM_001020825.2:c.2097A>C, NM_001020825.1:c.2097A>C, NM_001018077.1:c.2097A>C, NM_001364185.1:c.2100A>C, NM_001364182.1:c.2097A>C, NM_001018074.1:c.2097A>C, NM_001018075.1:c.2097A>C, NP_000167.1:p.Lys699Asn, NP_001019265.1:p.Lys700Asn, NP_001191193.1:p.Lys364Asn, NP_001191192.1:p.Lys369Asn, NP_001191191.1:p.Lys384Asn, NP_001191190.1:p.Lys602Asn, NP_001191189.1:p.Lys610Asn, NP_001191188.1:p.Lys614Asn, NP_001191187.1:p.Lys673Asn, NP_001351112.1:p.Lys700Asn, NP_001351110.1:p.Lys699Asn, NP_001351109.1:p.Lys699Asn, NP_001351113.1:p.Lys700Asn, NP_001018086.1:p.Lys699Asn, NP_001018661.1:p.Lys699Asn, NP_001018087.1:p.Lys699Asn, NP_001351114.1:p.Lys700Asn, NP_001351111.1:p.Lys699Asn, NP_001018084.1:p.Lys699Asn, NP_001018085.1:p.Lys699Asn

                8.

                rs1482933244 [Homo sapiens]
                  Variant type:
                  SNV
                  Alleles:
                  A>G [Show Flanks]
                  Chromosome:
                  5:143400207 (GRCh38)
                  5:142779772 (GRCh37)
                  Canonical SPDI:
                  NC_000005.10:143400206:A:G
                  Gene:
                  NR3C1 (Varview)
                  Functional Consequence:
                  5_prime_UTR_variant,intron_variant,synonymous_variant,coding_sequence_variant
                  Validated:
                  by frequency,by alfa,by cluster
                  MAF:
                  G=0.000028/1 (ALFA)
                  G=0.000004/1 (GnomAD_exomes)
                  G=0.000007/1 (GnomAD)
                  G=0.000008/2 (TOPMED)
                  HGVS:
                  NC_000005.10:g.143400207A>G, NC_000005.9:g.142779772A>G, NG_009062.1:g.40306T>C, NM_000176.3:c.633T>C, NM_000176.2:c.633T>C, NM_001024094.2:c.633T>C, NM_001024094.1:c.633T>C, NM_001204264.2:c.-373T>C, NM_001204264.1:c.-373T>C, NM_001204263.2:c.-358T>C, NM_001204263.1:c.-358T>C, NM_001204262.2:c.-313T>C, NM_001204262.1:c.-313T>C, NM_001204261.2:c.342T>C, NM_001204261.1:c.342T>C, NM_001204260.2:c.366T>C, NM_001204260.1:c.366T>C, NM_001204259.2:c.378T>C, NM_001204259.1:c.378T>C, NM_001204258.2:c.555T>C, NM_001204258.1:c.555T>C, NM_001364183.2:c.633T>C, NM_001364183.1:c.633T>C, NM_001364181.2:c.633T>C, NM_001364181.1:c.633T>C, NM_001364180.2:c.633T>C, NM_001364180.1:c.633T>C, NM_001364184.2:c.633T>C, NM_001364184.1:c.633T>C, NM_001018076.2:c.633T>C, NM_001018076.1:c.633T>C, NM_001020825.2:c.633T>C, NM_001020825.1:c.633T>C, NM_001204265.2:c.633T>C, NM_001204265.1:c.633T>C, NM_001018077.1:c.633T>C, NM_001364185.1:c.633T>C, NM_001364182.1:c.633T>C, NM_001018074.1:c.633T>C, NM_001018075.1:c.633T>C

                  9.

                  rs1477445177 [Homo sapiens]
                    Variant type:
                    SNV
                    Alleles:
                    G>A [Show Flanks]
                    Chromosome:
                    5:143400528 (GRCh38)
                    5:142780093 (GRCh37)
                    Canonical SPDI:
                    NC_000005.10:143400527:G:A
                    Gene:
                    NR3C1 (Varview)
                    Functional Consequence:
                    synonymous_variant,intron_variant,5_prime_UTR_variant,coding_sequence_variant
                    Validated:
                    by frequency
                    MAF:
                    A=0.000004/1 (GnomAD_exomes)
                    HGVS:
                    NC_000005.10:g.143400528G>A, NC_000005.9:g.142780093G>A, NG_009062.1:g.39985C>T, NM_000176.3:c.312C>T, NM_000176.2:c.312C>T, NM_001024094.2:c.312C>T, NM_001024094.1:c.312C>T, NM_001204264.2:c.-694C>T, NM_001204264.1:c.-694C>T, NM_001204263.2:c.-679C>T, NM_001204263.1:c.-679C>T, NM_001204262.2:c.-634C>T, NM_001204262.1:c.-634C>T, NM_001204261.2:c.21C>T, NM_001204261.1:c.21C>T, NM_001204260.2:c.45C>T, NM_001204260.1:c.45C>T, NM_001204259.2:c.57C>T, NM_001204259.1:c.57C>T, NM_001204258.2:c.234C>T, NM_001204258.1:c.234C>T, NM_001364183.2:c.312C>T, NM_001364183.1:c.312C>T, NM_001364181.2:c.312C>T, NM_001364181.1:c.312C>T, NM_001364180.2:c.312C>T, NM_001364180.1:c.312C>T, NM_001364184.2:c.312C>T, NM_001364184.1:c.312C>T, NM_001018076.2:c.312C>T, NM_001018076.1:c.312C>T, NM_001020825.2:c.312C>T, NM_001020825.1:c.312C>T, NM_001204265.2:c.312C>T, NM_001204265.1:c.312C>T, NM_001018077.1:c.312C>T, NM_001364185.1:c.312C>T, NM_001364182.1:c.312C>T, NM_001018074.1:c.312C>T, NM_001018075.1:c.312C>T

                    10.

                    rs1477383667 [Homo sapiens]
                      Variant type:
                      SNV
                      Alleles:
                      G>A,C [Show Flanks]
                      Chromosome:
                      5:143399886 (GRCh38)
                      5:142779451 (GRCh37)
                      Canonical SPDI:
                      NC_000005.10:143399885:G:A,NC_000005.10:143399885:G:C
                      Gene:
                      NR3C1 (Varview)
                      Functional Consequence:
                      synonymous_variant,intron_variant,5_prime_UTR_variant,coding_sequence_variant
                      Validated:
                      by frequency,by alfa,by cluster
                      MAF:
                      C=0./0 (ALFA)
                      A=0.000004/1 (GnomAD_exomes)
                      A=0.000071/1 (TOMMO)
                      HGVS:
                      NC_000005.10:g.143399886G>A, NC_000005.10:g.143399886G>C, NC_000005.9:g.142779451G>A, NC_000005.9:g.142779451G>C, NG_009062.1:g.40627C>T, NG_009062.1:g.40627C>G, NM_000176.3:c.954C>T, NM_000176.3:c.954C>G, NM_000176.2:c.954C>T, NM_000176.2:c.954C>G, NM_001024094.2:c.954C>T, NM_001024094.2:c.954C>G, NM_001024094.1:c.954C>T, NM_001024094.1:c.954C>G, NM_001204264.2:c.-52C>T, NM_001204264.2:c.-52C>G, NM_001204264.1:c.-52C>T, NM_001204264.1:c.-52C>G, NM_001204263.2:c.-37C>T, NM_001204263.2:c.-37C>G, NM_001204263.1:c.-37C>T, NM_001204263.1:c.-37C>G, NM_001204262.2:c.9C>T, NM_001204262.2:c.9C>G, NM_001204262.1:c.9C>T, NM_001204262.1:c.9C>G, NM_001204261.2:c.663C>T, NM_001204261.2:c.663C>G, NM_001204261.1:c.663C>T, NM_001204261.1:c.663C>G, NM_001204260.2:c.687C>T, NM_001204260.2:c.687C>G, NM_001204260.1:c.687C>T, NM_001204260.1:c.687C>G, NM_001204259.2:c.699C>T, NM_001204259.2:c.699C>G, NM_001204259.1:c.699C>T, NM_001204259.1:c.699C>G, NM_001204258.2:c.876C>T, NM_001204258.2:c.876C>G, NM_001204258.1:c.876C>T, NM_001204258.1:c.876C>G, NM_001364183.2:c.954C>T, NM_001364183.2:c.954C>G, NM_001364183.1:c.954C>T, NM_001364183.1:c.954C>G, NM_001364181.2:c.954C>T, NM_001364181.2:c.954C>G, NM_001364181.1:c.954C>T, NM_001364181.1:c.954C>G, NM_001364180.2:c.954C>T, NM_001364180.2:c.954C>G, NM_001364180.1:c.954C>T, NM_001364180.1:c.954C>G, NM_001364184.2:c.954C>T, NM_001364184.2:c.954C>G, NM_001364184.1:c.954C>T, NM_001364184.1:c.954C>G, NM_001018076.2:c.954C>T, NM_001018076.2:c.954C>G, NM_001018076.1:c.954C>T, NM_001018076.1:c.954C>G, NM_001020825.2:c.954C>T, NM_001020825.2:c.954C>G, NM_001020825.1:c.954C>T, NM_001020825.1:c.954C>G, NM_001204265.2:c.954C>T, NM_001204265.2:c.954C>G, NM_001204265.1:c.954C>T, NM_001204265.1:c.954C>G, NM_001018077.1:c.954C>T, NM_001018077.1:c.954C>G, NM_001364185.1:c.954C>T, NM_001364185.1:c.954C>G, NM_001364182.1:c.954C>T, NM_001364182.1:c.954C>G, NM_001018074.1:c.954C>T, NM_001018074.1:c.954C>G, NM_001018075.1:c.954C>T, NM_001018075.1:c.954C>G

                      11.

                      rs1474609295 [Homo sapiens]
                        Variant type:
                        SNV
                        Alleles:
                        C>T [Show Flanks]
                        Chromosome:
                        5:143400152 (GRCh38)
                        5:142779717 (GRCh37)
                        Canonical SPDI:
                        NC_000005.10:143400151:C:T
                        Gene:
                        NR3C1 (Varview)
                        Functional Consequence:
                        intron_variant,5_prime_UTR_variant,coding_sequence_variant,missense_variant
                        Validated:
                        by frequency,by alfa
                        MAF:
                        T=0./0 (ALFA)
                        T=0.000004/1 (GnomAD_exomes)
                        HGVS:
                        NC_000005.10:g.143400152C>T, NC_000005.9:g.142779717C>T, NG_009062.1:g.40361G>A, NM_000176.3:c.688G>A, NM_000176.2:c.688G>A, NM_001024094.2:c.688G>A, NM_001024094.1:c.688G>A, NM_001204264.2:c.-318G>A, NM_001204264.1:c.-318G>A, NM_001204263.2:c.-303G>A, NM_001204263.1:c.-303G>A, NM_001204262.2:c.-258G>A, NM_001204262.1:c.-258G>A, NM_001204261.2:c.397G>A, NM_001204261.1:c.397G>A, NM_001204260.2:c.421G>A, NM_001204260.1:c.421G>A, NM_001204259.2:c.433G>A, NM_001204259.1:c.433G>A, NM_001204258.2:c.610G>A, NM_001204258.1:c.610G>A, NM_001364183.2:c.688G>A, NM_001364183.1:c.688G>A, NM_001364181.2:c.688G>A, NM_001364181.1:c.688G>A, NM_001364180.2:c.688G>A, NM_001364180.1:c.688G>A, NM_001364184.2:c.688G>A, NM_001364184.1:c.688G>A, NM_001018076.2:c.688G>A, NM_001018076.1:c.688G>A, NM_001020825.2:c.688G>A, NM_001020825.1:c.688G>A, NM_001204265.2:c.688G>A, NM_001204265.1:c.688G>A, NM_001018077.1:c.688G>A, NM_001364185.1:c.688G>A, NM_001364182.1:c.688G>A, NM_001018074.1:c.688G>A, NM_001018075.1:c.688G>A, NP_000167.1:p.Gly230Arg, NP_001019265.1:p.Gly230Arg, NP_001191190.1:p.Gly133Arg, NP_001191189.1:p.Gly141Arg, NP_001191188.1:p.Gly145Arg, NP_001191187.1:p.Gly204Arg, NP_001351112.1:p.Gly230Arg, NP_001351110.1:p.Gly230Arg, NP_001351109.1:p.Gly230Arg, NP_001351113.1:p.Gly230Arg, NP_001018086.1:p.Gly230Arg, NP_001018661.1:p.Gly230Arg, NP_001191194.1:p.Gly230Arg, NP_001018087.1:p.Gly230Arg, NP_001351114.1:p.Gly230Arg, NP_001351111.1:p.Gly230Arg, NP_001018084.1:p.Gly230Arg, NP_001018085.1:p.Gly230Arg

                        12.

                        rs1473567916 [Homo sapiens]
                          Variant type:
                          SNV
                          Alleles:
                          T>C [Show Flanks]
                          Chromosome:
                          5:143400458 (GRCh38)
                          5:142780023 (GRCh37)
                          Canonical SPDI:
                          NC_000005.10:143400457:T:C
                          Gene:
                          NR3C1 (Varview)
                          Functional Consequence:
                          intron_variant,5_prime_UTR_variant,coding_sequence_variant,missense_variant
                          Validated:
                          by frequency,by alfa,by cluster
                          MAF:
                          C=0.000031/1 (ALFA)
                          C=0.000004/1 (GnomAD_exomes)
                          C=0.000008/2 (TOPMED)
                          HGVS:
                          NC_000005.10:g.143400458T>C, NC_000005.9:g.142780023T>C, NG_009062.1:g.40055A>G, NM_000176.3:c.382A>G, NM_000176.2:c.382A>G, NM_001024094.2:c.382A>G, NM_001024094.1:c.382A>G, NM_001204264.2:c.-624A>G, NM_001204264.1:c.-624A>G, NM_001204263.2:c.-609A>G, NM_001204263.1:c.-609A>G, NM_001204262.2:c.-564A>G, NM_001204262.1:c.-564A>G, NM_001204261.2:c.91A>G, NM_001204261.1:c.91A>G, NM_001204260.2:c.115A>G, NM_001204260.1:c.115A>G, NM_001204259.2:c.127A>G, NM_001204259.1:c.127A>G, NM_001204258.2:c.304A>G, NM_001204258.1:c.304A>G, NM_001364183.2:c.382A>G, NM_001364183.1:c.382A>G, NM_001364181.2:c.382A>G, NM_001364181.1:c.382A>G, NM_001364180.2:c.382A>G, NM_001364180.1:c.382A>G, NM_001364184.2:c.382A>G, NM_001364184.1:c.382A>G, NM_001018076.2:c.382A>G, NM_001018076.1:c.382A>G, NM_001020825.2:c.382A>G, NM_001020825.1:c.382A>G, NM_001204265.2:c.382A>G, NM_001204265.1:c.382A>G, NM_001018077.1:c.382A>G, NM_001364185.1:c.382A>G, NM_001364182.1:c.382A>G, NM_001018074.1:c.382A>G, NM_001018075.1:c.382A>G, NP_000167.1:p.Asn128Asp, NP_001019265.1:p.Asn128Asp, NP_001191190.1:p.Asn31Asp, NP_001191189.1:p.Asn39Asp, NP_001191188.1:p.Asn43Asp, NP_001191187.1:p.Asn102Asp, NP_001351112.1:p.Asn128Asp, NP_001351110.1:p.Asn128Asp, NP_001351109.1:p.Asn128Asp, NP_001351113.1:p.Asn128Asp, NP_001018086.1:p.Asn128Asp, NP_001018661.1:p.Asn128Asp, NP_001191194.1:p.Asn128Asp, NP_001018087.1:p.Asn128Asp, NP_001351114.1:p.Asn128Asp, NP_001351111.1:p.Asn128Asp, NP_001018084.1:p.Asn128Asp, NP_001018085.1:p.Asn128Asp

                          13.

                          rs1473178782 [Homo sapiens]
                            Variant type:
                            SNV
                            Alleles:
                            A>G [Show Flanks]
                            Chromosome:
                            5:143310167 (GRCh38)
                            5:142689732 (GRCh37)
                            Canonical SPDI:
                            NC_000005.10:143310166:A:G
                            Gene:
                            NR3C1 (Varview)
                            Functional Consequence:
                            non_coding_transcript_variant,synonymous_variant,coding_sequence_variant
                            Validated:
                            by frequency
                            MAF:
                            G=0.000004/1 (GnomAD_exomes)
                            HGVS:
                            NC_000005.10:g.143310167A>G, NC_000005.9:g.142689732A>G, NG_009062.1:g.130346T>C, NM_000176.3:c.1398T>C, NM_000176.2:c.1398T>C, NM_001024094.2:c.1401T>C, NM_001024094.1:c.1401T>C, NM_001204264.2:c.393T>C, NM_001204264.1:c.393T>C, NM_001204263.2:c.408T>C, NM_001204263.1:c.408T>C, NM_001204262.2:c.453T>C, NM_001204262.1:c.453T>C, NM_001204261.2:c.1107T>C, NM_001204261.1:c.1107T>C, NM_001204260.2:c.1131T>C, NM_001204260.1:c.1131T>C, NM_001204259.2:c.1143T>C, NM_001204259.1:c.1143T>C, NM_001204258.2:c.1320T>C, NM_001204258.1:c.1320T>C, NM_001364183.2:c.1401T>C, NM_001364183.1:c.1401T>C, NM_001364181.2:c.1398T>C, NM_001364181.1:c.1398T>C, NM_001364180.2:c.1398T>C, NM_001364180.1:c.1398T>C, NM_001364184.2:c.1401T>C, NM_001364184.1:c.1401T>C, NM_001018076.2:c.1398T>C, NM_001018076.1:c.1398T>C, NR_157096.2:n.321T>C, NR_157096.1:n.321T>C, NM_001020825.2:c.1398T>C, NM_001020825.1:c.1398T>C, NM_001204265.2:c.1398T>C, NM_001204265.1:c.1398T>C, NM_001018077.1:c.1398T>C, NM_001364185.1:c.1401T>C, NM_001364182.1:c.1398T>C, NM_001018074.1:c.1398T>C, NM_001018075.1:c.1398T>C

                            14.

                            rs1470677560 [Homo sapiens]
                              Variant type:
                              SNV
                              Alleles:
                              C>A,T [Show Flanks]
                              Chromosome:
                              5:143282623 (GRCh38)
                              5:142662188 (GRCh37)
                              Canonical SPDI:
                              NC_000005.10:143282622:C:A,NC_000005.10:143282622:C:T
                              Gene:
                              NR3C1 (Varview)
                              Functional Consequence:
                              non_coding_transcript_variant,genic_downstream_transcript_variant,missense_variant,coding_sequence_variant
                              Validated:
                              by frequency,by alfa,by cluster
                              MAF:
                              T=0./0 (ALFA)
                              T=0.000008/2 (TOPMED)
                              HGVS:
                              NC_000005.10:g.143282623C>A, NC_000005.10:g.143282623C>T, NC_000005.9:g.142662188C>A, NC_000005.9:g.142662188C>T, NG_009062.1:g.157890G>T, NG_009062.1:g.157890G>A, NM_000176.3:c.2126G>T, NM_000176.3:c.2126G>A, NM_000176.2:c.2126G>T, NM_000176.2:c.2126G>A, NM_001024094.2:c.2129G>T, NM_001024094.2:c.2129G>A, NM_001024094.1:c.2129G>T, NM_001024094.1:c.2129G>A, NM_001204264.2:c.1121G>T, NM_001204264.2:c.1121G>A, NM_001204264.1:c.1121G>T, NM_001204264.1:c.1121G>A, NM_001204263.2:c.1136G>T, NM_001204263.2:c.1136G>A, NM_001204263.1:c.1136G>T, NM_001204263.1:c.1136G>A, NM_001204262.2:c.1181G>T, NM_001204262.2:c.1181G>A, NM_001204262.1:c.1181G>T, NM_001204262.1:c.1181G>A, NM_001204261.2:c.1835G>T, NM_001204261.2:c.1835G>A, NM_001204261.1:c.1835G>T, NM_001204261.1:c.1835G>A, NM_001204260.2:c.1859G>T, NM_001204260.2:c.1859G>A, NM_001204260.1:c.1859G>T, NM_001204260.1:c.1859G>A, NM_001204259.2:c.1871G>T, NM_001204259.2:c.1871G>A, NM_001204259.1:c.1871G>T, NM_001204259.1:c.1871G>A, NM_001204258.2:c.2048G>T, NM_001204258.2:c.2048G>A, NM_001204258.1:c.2048G>T, NM_001204258.1:c.2048G>A, NM_001364183.2:c.2129G>T, NM_001364183.2:c.2129G>A, NM_001364183.1:c.2129G>T, NM_001364183.1:c.2129G>A, NM_001364181.2:c.2126G>T, NM_001364181.2:c.2126G>A, NM_001364181.1:c.2126G>T, NM_001364181.1:c.2126G>A, NM_001364180.2:c.2126G>T, NM_001364180.2:c.2126G>A, NM_001364180.1:c.2126G>T, NM_001364180.1:c.2126G>A, NM_001364184.2:c.2129G>T, NM_001364184.2:c.2129G>A, NM_001364184.1:c.2129G>T, NM_001364184.1:c.2129G>A, NM_001018076.2:c.2126G>T, NM_001018076.2:c.2126G>A, NM_001018076.1:c.2126G>T, NM_001018076.1:c.2126G>A, NR_157096.2:n.1049G>T, NR_157096.2:n.1049G>A, NR_157096.1:n.1049G>T, NR_157096.1:n.1049G>A, NM_001020825.2:c.2126G>T, NM_001020825.2:c.2126G>A, NM_001020825.1:c.2126G>T, NM_001020825.1:c.2126G>A, NM_001018077.1:c.2126G>T, NM_001018077.1:c.2126G>A, NM_001364185.1:c.2129G>T, NM_001364185.1:c.2129G>A, NM_001364182.1:c.2126G>T, NM_001364182.1:c.2126G>A, NM_001018074.1:c.2126G>T, NM_001018074.1:c.2126G>A, NM_001018075.1:c.2126G>T, NM_001018075.1:c.2126G>A, NP_000167.1:p.Ser709Ile, NP_000167.1:p.Ser709Asn, NP_001019265.1:p.Ser710Ile, NP_001019265.1:p.Ser710Asn, NP_001191193.1:p.Ser374Ile, NP_001191193.1:p.Ser374Asn, NP_001191192.1:p.Ser379Ile, NP_001191192.1:p.Ser379Asn, NP_001191191.1:p.Ser394Ile, NP_001191191.1:p.Ser394Asn, NP_001191190.1:p.Ser612Ile, NP_001191190.1:p.Ser612Asn, NP_001191189.1:p.Ser620Ile, NP_001191189.1:p.Ser620Asn, NP_001191188.1:p.Ser624Ile, NP_001191188.1:p.Ser624Asn, NP_001191187.1:p.Ser683Ile, NP_001191187.1:p.Ser683Asn, NP_001351112.1:p.Ser710Ile, NP_001351112.1:p.Ser710Asn, NP_001351110.1:p.Ser709Ile, NP_001351110.1:p.Ser709Asn, NP_001351109.1:p.Ser709Ile, NP_001351109.1:p.Ser709Asn, NP_001351113.1:p.Ser710Ile, NP_001351113.1:p.Ser710Asn, NP_001018086.1:p.Ser709Ile, NP_001018086.1:p.Ser709Asn, NP_001018661.1:p.Ser709Ile, NP_001018661.1:p.Ser709Asn, NP_001018087.1:p.Ser709Ile, NP_001018087.1:p.Ser709Asn, NP_001351114.1:p.Ser710Ile, NP_001351114.1:p.Ser710Asn, NP_001351111.1:p.Ser709Ile, NP_001351111.1:p.Ser709Asn, NP_001018084.1:p.Ser709Ile, NP_001018084.1:p.Ser709Asn, NP_001018085.1:p.Ser709Ile, NP_001018085.1:p.Ser709Asn

                              15.

                              rs1468878454 [Homo sapiens]
                                Variant type:
                                SNV
                                Alleles:
                                T>C,G [Show Flanks]
                                Chromosome:
                                5:143314135 (GRCh38)
                                5:142693700 (GRCh37)
                                Canonical SPDI:
                                NC_000005.10:143314134:T:C,NC_000005.10:143314134:T:G
                                Gene:
                                NR3C1 (Varview)
                                Functional Consequence:
                                synonymous_variant,non_coding_transcript_variant,coding_sequence_variant
                                Validated:
                                by frequency,by alfa,by cluster
                                MAF:
                                G=0./0 (ALFA)
                                G=0.000008/2 (GnomAD_exomes)
                                HGVS:
                                NC_000005.10:g.143314135T>C, NC_000005.10:g.143314135T>G, NC_000005.9:g.142693700T>C, NC_000005.9:g.142693700T>G, NG_009062.1:g.126378A>G, NG_009062.1:g.126378A>C, NM_000176.3:c.1218A>G, NM_000176.3:c.1218A>C, NM_000176.2:c.1218A>G, NM_000176.2:c.1218A>C, NM_001024094.2:c.1218A>G, NM_001024094.2:c.1218A>C, NM_001024094.1:c.1218A>G, NM_001024094.1:c.1218A>C, NM_001204264.2:c.213A>G, NM_001204264.2:c.213A>C, NM_001204264.1:c.213A>G, NM_001204264.1:c.213A>C, NM_001204263.2:c.228A>G, NM_001204263.2:c.228A>C, NM_001204263.1:c.228A>G, NM_001204263.1:c.228A>C, NM_001204262.2:c.273A>G, NM_001204262.2:c.273A>C, NM_001204262.1:c.273A>G, NM_001204262.1:c.273A>C, NM_001204261.2:c.927A>G, NM_001204261.2:c.927A>C, NM_001204261.1:c.927A>G, NM_001204261.1:c.927A>C, NM_001204260.2:c.951A>G, NM_001204260.2:c.951A>C, NM_001204260.1:c.951A>G, NM_001204260.1:c.951A>C, NM_001204259.2:c.963A>G, NM_001204259.2:c.963A>C, NM_001204259.1:c.963A>G, NM_001204259.1:c.963A>C, NM_001204258.2:c.1140A>G, NM_001204258.2:c.1140A>C, NM_001204258.1:c.1140A>G, NM_001204258.1:c.1140A>C, NM_001364183.2:c.1218A>G, NM_001364183.2:c.1218A>C, NM_001364183.1:c.1218A>G, NM_001364183.1:c.1218A>C, NM_001364181.2:c.1218A>G, NM_001364181.2:c.1218A>C, NM_001364181.1:c.1218A>G, NM_001364181.1:c.1218A>C, NM_001364180.2:c.1218A>G, NM_001364180.2:c.1218A>C, NM_001364180.1:c.1218A>G, NM_001364180.1:c.1218A>C, NM_001364184.2:c.1218A>G, NM_001364184.2:c.1218A>C, NM_001364184.1:c.1218A>G, NM_001364184.1:c.1218A>C, NM_001018076.2:c.1218A>G, NM_001018076.2:c.1218A>C, NM_001018076.1:c.1218A>G, NM_001018076.1:c.1218A>C, NR_157096.2:n.141A>G, NR_157096.2:n.141A>C, NR_157096.1:n.141A>G, NR_157096.1:n.141A>C, NM_001020825.2:c.1218A>G, NM_001020825.2:c.1218A>C, NM_001020825.1:c.1218A>G, NM_001020825.1:c.1218A>C, NM_001204265.2:c.1218A>G, NM_001204265.2:c.1218A>C, NM_001204265.1:c.1218A>G, NM_001204265.1:c.1218A>C, NM_001018077.1:c.1218A>G, NM_001018077.1:c.1218A>C, NM_001364185.1:c.1218A>G, NM_001364185.1:c.1218A>C, NM_001364182.1:c.1218A>G, NM_001364182.1:c.1218A>C, NM_001018074.1:c.1218A>G, NM_001018074.1:c.1218A>C, NM_001018075.1:c.1218A>G, NM_001018075.1:c.1218A>C

                                16.

                                rs1468341591 [Homo sapiens]
                                  Variant type:
                                  SNV
                                  Alleles:
                                  G>C [Show Flanks]
                                  Chromosome:
                                  5:143399819 (GRCh38)
                                  5:142779384 (GRCh37)
                                  Canonical SPDI:
                                  NC_000005.10:143399818:G:C
                                  Gene:
                                  NR3C1 (Varview)
                                  Functional Consequence:
                                  missense_variant,intron_variant,coding_sequence_variant
                                  Validated:
                                  by frequency
                                  MAF:
                                  C=0.000004/1 (GnomAD_exomes)
                                  HGVS:
                                  NC_000005.10:g.143399819G>C, NC_000005.9:g.142779384G>C, NG_009062.1:g.40694C>G, NM_000176.3:c.1021C>G, NM_000176.2:c.1021C>G, NM_001024094.2:c.1021C>G, NM_001024094.1:c.1021C>G, NM_001204264.2:c.16C>G, NM_001204264.1:c.16C>G, NM_001204263.2:c.31C>G, NM_001204263.1:c.31C>G, NM_001204262.2:c.76C>G, NM_001204262.1:c.76C>G, NM_001204261.2:c.730C>G, NM_001204261.1:c.730C>G, NM_001204260.2:c.754C>G, NM_001204260.1:c.754C>G, NM_001204259.2:c.766C>G, NM_001204259.1:c.766C>G, NM_001204258.2:c.943C>G, NM_001204258.1:c.943C>G, NM_001364183.2:c.1021C>G, NM_001364183.1:c.1021C>G, NM_001364181.2:c.1021C>G, NM_001364181.1:c.1021C>G, NM_001364180.2:c.1021C>G, NM_001364180.1:c.1021C>G, NM_001364184.2:c.1021C>G, NM_001364184.1:c.1021C>G, NM_001018076.2:c.1021C>G, NM_001018076.1:c.1021C>G, NM_001020825.2:c.1021C>G, NM_001020825.1:c.1021C>G, NM_001204265.2:c.1021C>G, NM_001204265.1:c.1021C>G, NM_001018077.1:c.1021C>G, NM_001364185.1:c.1021C>G, NM_001364182.1:c.1021C>G, NM_001018074.1:c.1021C>G, NM_001018075.1:c.1021C>G, NP_000167.1:p.Leu341Val, NP_001019265.1:p.Leu341Val, NP_001191193.1:p.Leu6Val, NP_001191192.1:p.Leu11Val, NP_001191191.1:p.Leu26Val, NP_001191190.1:p.Leu244Val, NP_001191189.1:p.Leu252Val, NP_001191188.1:p.Leu256Val, NP_001191187.1:p.Leu315Val, NP_001351112.1:p.Leu341Val, NP_001351110.1:p.Leu341Val, NP_001351109.1:p.Leu341Val, NP_001351113.1:p.Leu341Val, NP_001018086.1:p.Leu341Val, NP_001018661.1:p.Leu341Val, NP_001191194.1:p.Leu341Val, NP_001018087.1:p.Leu341Val, NP_001351114.1:p.Leu341Val, NP_001351111.1:p.Leu341Val, NP_001018084.1:p.Leu341Val, NP_001018085.1:p.Leu341Val

                                  17.

                                  rs1466324542 [Homo sapiens]
                                    Variant type:
                                    SNV
                                    Alleles:
                                    G>A [Show Flanks]
                                    Chromosome:
                                    5:143300661 (GRCh38)
                                    5:142680226 (GRCh37)
                                    Canonical SPDI:
                                    NC_000005.10:143300660:G:A
                                    Gene:
                                    NR3C1 (Varview)
                                    Functional Consequence:
                                    missense_variant,non_coding_transcript_variant,coding_sequence_variant
                                    Validated:
                                    by frequency,by alfa
                                    MAF:
                                    A=0./0 (ALFA)
                                    A=0.000004/1 (TOPMED)
                                    HGVS:
                                    NC_000005.10:g.143300661G>A, NC_000005.9:g.142680226G>A, NG_009062.1:g.139852C>T, NM_000176.3:c.1571C>T, NM_000176.2:c.1571C>T, NM_001024094.2:c.1574C>T, NM_001024094.1:c.1574C>T, NM_001204264.2:c.566C>T, NM_001204264.1:c.566C>T, NM_001204263.2:c.581C>T, NM_001204263.1:c.581C>T, NM_001204262.2:c.626C>T, NM_001204262.1:c.626C>T, NM_001204261.2:c.1280C>T, NM_001204261.1:c.1280C>T, NM_001204260.2:c.1304C>T, NM_001204260.1:c.1304C>T, NM_001204259.2:c.1316C>T, NM_001204259.1:c.1316C>T, NM_001204258.2:c.1493C>T, NM_001204258.1:c.1493C>T, NM_001364183.2:c.1574C>T, NM_001364183.1:c.1574C>T, NM_001364181.2:c.1571C>T, NM_001364181.1:c.1571C>T, NM_001364180.2:c.1571C>T, NM_001364180.1:c.1571C>T, NM_001364184.2:c.1574C>T, NM_001364184.1:c.1574C>T, NM_001018076.2:c.1571C>T, NM_001018076.1:c.1571C>T, NR_157096.2:n.494C>T, NR_157096.1:n.494C>T, NM_001020825.2:c.1571C>T, NM_001020825.1:c.1571C>T, NM_001204265.2:c.1571C>T, NM_001204265.1:c.1571C>T, NM_001018077.1:c.1571C>T, NM_001364185.1:c.1574C>T, NM_001364182.1:c.1571C>T, NM_001018074.1:c.1571C>T, NM_001018075.1:c.1571C>T, NP_000167.1:p.Thr524Met, NP_001019265.1:p.Thr525Met, NP_001191193.1:p.Thr189Met, NP_001191192.1:p.Thr194Met, NP_001191191.1:p.Thr209Met, NP_001191190.1:p.Thr427Met, NP_001191189.1:p.Thr435Met, NP_001191188.1:p.Thr439Met, NP_001191187.1:p.Thr498Met, NP_001351112.1:p.Thr525Met, NP_001351110.1:p.Thr524Met, NP_001351109.1:p.Thr524Met, NP_001351113.1:p.Thr525Met, NP_001018086.1:p.Thr524Met, NP_001018661.1:p.Thr524Met, NP_001191194.1:p.Thr524Met, NP_001018087.1:p.Thr524Met, NP_001351114.1:p.Thr525Met, NP_001351111.1:p.Thr524Met, NP_001018084.1:p.Thr524Met, NP_001018085.1:p.Thr524Met

                                    18.

                                    rs1465201623 [Homo sapiens]
                                      Variant type:
                                      SNV
                                      Alleles:
                                      A>G [Show Flanks]
                                      Chromosome:
                                      5:143400476 (GRCh38)
                                      5:142780041 (GRCh37)
                                      Canonical SPDI:
                                      NC_000005.10:143400475:A:G
                                      Gene:
                                      NR3C1 (Varview)
                                      Functional Consequence:
                                      synonymous_variant,intron_variant,5_prime_UTR_variant,coding_sequence_variant
                                      Validated:
                                      by frequency,by cluster
                                      MAF:
                                      G=0.000004/1 (GnomAD_exomes)
                                      G=0.000007/1 (GnomAD)
                                      HGVS:
                                      NC_000005.10:g.143400476A>G, NC_000005.9:g.142780041A>G, NG_009062.1:g.40037T>C, NM_000176.3:c.364T>C, NM_000176.2:c.364T>C, NM_001024094.2:c.364T>C, NM_001024094.1:c.364T>C, NM_001204264.2:c.-642T>C, NM_001204264.1:c.-642T>C, NM_001204263.2:c.-627T>C, NM_001204263.1:c.-627T>C, NM_001204262.2:c.-582T>C, NM_001204262.1:c.-582T>C, NM_001204261.2:c.73T>C, NM_001204261.1:c.73T>C, NM_001204260.2:c.97T>C, NM_001204260.1:c.97T>C, NM_001204259.2:c.109T>C, NM_001204259.1:c.109T>C, NM_001204258.2:c.286T>C, NM_001204258.1:c.286T>C, NM_001364183.2:c.364T>C, NM_001364183.1:c.364T>C, NM_001364181.2:c.364T>C, NM_001364181.1:c.364T>C, NM_001364180.2:c.364T>C, NM_001364180.1:c.364T>C, NM_001364184.2:c.364T>C, NM_001364184.1:c.364T>C, NM_001018076.2:c.364T>C, NM_001018076.1:c.364T>C, NM_001020825.2:c.364T>C, NM_001020825.1:c.364T>C, NM_001204265.2:c.364T>C, NM_001204265.1:c.364T>C, NM_001018077.1:c.364T>C, NM_001364185.1:c.364T>C, NM_001364182.1:c.364T>C, NM_001018074.1:c.364T>C, NM_001018075.1:c.364T>C

                                      19.

                                      rs1462285938 [Homo sapiens]
                                        Variant type:
                                        SNV
                                        Alleles:
                                        G>T [Show Flanks]
                                        Chromosome:
                                        5:143399773 (GRCh38)
                                        5:142779338 (GRCh37)
                                        Canonical SPDI:
                                        NC_000005.10:143399772:G:T
                                        Gene:
                                        NR3C1 (Varview)
                                        Functional Consequence:
                                        missense_variant,intron_variant,coding_sequence_variant
                                        Validated:
                                        by frequency,by alfa
                                        MAF:
                                        T=0.000047/1 (ALFA)
                                        T=0.000004/1 (GnomAD_exomes)
                                        HGVS:
                                        NC_000005.10:g.143399773G>T, NC_000005.9:g.142779338G>T, NG_009062.1:g.40740C>A, NM_000176.3:c.1067C>A, NM_000176.2:c.1067C>A, NM_001024094.2:c.1067C>A, NM_001024094.1:c.1067C>A, NM_001204264.2:c.62C>A, NM_001204264.1:c.62C>A, NM_001204263.2:c.77C>A, NM_001204263.1:c.77C>A, NM_001204262.2:c.122C>A, NM_001204262.1:c.122C>A, NM_001204261.2:c.776C>A, NM_001204261.1:c.776C>A, NM_001204260.2:c.800C>A, NM_001204260.1:c.800C>A, NM_001204259.2:c.812C>A, NM_001204259.1:c.812C>A, NM_001204258.2:c.989C>A, NM_001204258.1:c.989C>A, NM_001364183.2:c.1067C>A, NM_001364183.1:c.1067C>A, NM_001364181.2:c.1067C>A, NM_001364181.1:c.1067C>A, NM_001364180.2:c.1067C>A, NM_001364180.1:c.1067C>A, NM_001364184.2:c.1067C>A, NM_001364184.1:c.1067C>A, NM_001018076.2:c.1067C>A, NM_001018076.1:c.1067C>A, NM_001020825.2:c.1067C>A, NM_001020825.1:c.1067C>A, NM_001204265.2:c.1067C>A, NM_001204265.1:c.1067C>A, NM_001018077.1:c.1067C>A, NM_001364185.1:c.1067C>A, NM_001364182.1:c.1067C>A, NM_001018074.1:c.1067C>A, NM_001018075.1:c.1067C>A, NP_000167.1:p.Pro356Gln, NP_001019265.1:p.Pro356Gln, NP_001191193.1:p.Pro21Gln, NP_001191192.1:p.Pro26Gln, NP_001191191.1:p.Pro41Gln, NP_001191190.1:p.Pro259Gln, NP_001191189.1:p.Pro267Gln, NP_001191188.1:p.Pro271Gln, NP_001191187.1:p.Pro330Gln, NP_001351112.1:p.Pro356Gln, NP_001351110.1:p.Pro356Gln, NP_001351109.1:p.Pro356Gln, NP_001351113.1:p.Pro356Gln, NP_001018086.1:p.Pro356Gln, NP_001018661.1:p.Pro356Gln, NP_001191194.1:p.Pro356Gln, NP_001018087.1:p.Pro356Gln, NP_001351114.1:p.Pro356Gln, NP_001351111.1:p.Pro356Gln, NP_001018084.1:p.Pro356Gln, NP_001018085.1:p.Pro356Gln

                                        20.

                                        rs1461639820 [Homo sapiens]
                                          Variant type:
                                          SNV
                                          Alleles:
                                          T>C [Show Flanks]
                                          Chromosome:
                                          5:143400200 (GRCh38)
                                          5:142779765 (GRCh37)
                                          Canonical SPDI:
                                          NC_000005.10:143400199:T:C
                                          Gene:
                                          NR3C1 (Varview)
                                          Functional Consequence:
                                          missense_variant,intron_variant,5_prime_UTR_variant,coding_sequence_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_000005.10:g.143400200T>C, NC_000005.9:g.142779765T>C, NG_009062.1:g.40313A>G, NM_000176.3:c.640A>G, NM_000176.2:c.640A>G, NM_001024094.2:c.640A>G, NM_001024094.1:c.640A>G, NM_001204264.2:c.-366A>G, NM_001204264.1:c.-366A>G, NM_001204263.2:c.-351A>G, NM_001204263.1:c.-351A>G, NM_001204262.2:c.-306A>G, NM_001204262.1:c.-306A>G, NM_001204261.2:c.349A>G, NM_001204261.1:c.349A>G, NM_001204260.2:c.373A>G, NM_001204260.1:c.373A>G, NM_001204259.2:c.385A>G, NM_001204259.1:c.385A>G, NM_001204258.2:c.562A>G, NM_001204258.1:c.562A>G, NM_001364183.2:c.640A>G, NM_001364183.1:c.640A>G, NM_001364181.2:c.640A>G, NM_001364181.1:c.640A>G, NM_001364180.2:c.640A>G, NM_001364180.1:c.640A>G, NM_001364184.2:c.640A>G, NM_001364184.1:c.640A>G, NM_001018076.2:c.640A>G, NM_001018076.1:c.640A>G, NM_001020825.2:c.640A>G, NM_001020825.1:c.640A>G, NM_001204265.2:c.640A>G, NM_001204265.1:c.640A>G, NM_001018077.1:c.640A>G, NM_001364185.1:c.640A>G, NM_001364182.1:c.640A>G, NM_001018074.1:c.640A>G, NM_001018075.1:c.640A>G, NP_000167.1:p.Arg214Gly, NP_001019265.1:p.Arg214Gly, NP_001191190.1:p.Arg117Gly, NP_001191189.1:p.Arg125Gly, NP_001191188.1:p.Arg129Gly, NP_001191187.1:p.Arg188Gly, NP_001351112.1:p.Arg214Gly, NP_001351110.1:p.Arg214Gly, NP_001351109.1:p.Arg214Gly, NP_001351113.1:p.Arg214Gly, NP_001018086.1:p.Arg214Gly, NP_001018661.1:p.Arg214Gly, NP_001191194.1:p.Arg214Gly, NP_001018087.1:p.Arg214Gly, NP_001351114.1:p.Arg214Gly, NP_001351111.1:p.Arg214Gly, NP_001018084.1:p.Arg214Gly, NP_001018085.1:p.Arg214Gly

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