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Items: 1 to 20 of 624

1.

rs1491523220 has merged into rs3055442 [Homo sapiens]
    Variant type:
    DELINS
    Alleles:
    ACACACACACACAC>-,AC,ACAC,ACACAC,ACACACAC,ACACACACAC,ACACACACACAC,ACACACACACACACAC,ACACACACACACACACAC,ACACACACACACACACACAC,ACACACACACACACACACACAC,ACACACACACACACACACACACAC,ACACACACACACACACACACACACAC,ACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACACACACACAC [Show Flanks]
    Chromosome:
    12:10398374 (GRCh38)
    12:10550973 (GRCh37)
    Canonical SPDI:
    NC_000012.12:10398356:CACACACACACACACACACACACACACACAC:CACACACACACACACAC,NC_000012.12:10398356:CACACACACACACACACACACACACACACAC:CACACACACACACACACAC,NC_000012.12:10398356:CACACACACACACACACACACACACACACAC:CACACACACACACACACACAC,NC_000012.12:10398356:CACACACACACACACACACACACACACACAC:CACACACACACACACACACACAC,NC_000012.12:10398356:CACACACACACACACACACACACACACACAC:CACACACACACACACACACACACAC,NC_000012.12:10398356:CACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACAC,NC_000012.12:10398356:CACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACAC,NC_000012.12:10398356:CACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACAC,NC_000012.12:10398356:CACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACAC,NC_000012.12:10398356:CACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACAC,NC_000012.12:10398356:CACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACAC,NC_000012.12:10398356:CACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACACAC,NC_000012.12:10398356:CACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACACACAC,NC_000012.12:10398356:CACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACACACACAC,NC_000012.12:10398356:CACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACACACACACAC,NC_000012.12:10398356:CACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACACACACACACAC,NC_000012.12:10398356:CACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACACACACACACACACACAC
    Gene:
    KLRC4-KLRK1 (Varview), KLRK1-AS1 (Varview)
    Functional Consequence:
    intron_variant,non_coding_transcript_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    CACACACACACACACACAC=0./0 (ALFA)
    CA=0.4587/2297 (1000Genomes)
    HGVS:
    NC_000012.12:g.10398358AC[8], NC_000012.12:g.10398358AC[9], NC_000012.12:g.10398358AC[10], NC_000012.12:g.10398358AC[11], NC_000012.12:g.10398358AC[12], NC_000012.12:g.10398358AC[13], NC_000012.12:g.10398358AC[14], NC_000012.12:g.10398358AC[16], NC_000012.12:g.10398358AC[17], NC_000012.12:g.10398358AC[18], NC_000012.12:g.10398358AC[19], NC_000012.12:g.10398358AC[20], NC_000012.12:g.10398358AC[21], NC_000012.12:g.10398358AC[22], NC_000012.12:g.10398358AC[23], NC_000012.12:g.10398358AC[24], NC_000012.12:g.10398358AC[27], NC_000012.11:g.10550957AC[8], NC_000012.11:g.10550957AC[9], NC_000012.11:g.10550957AC[10], NC_000012.11:g.10550957AC[11], NC_000012.11:g.10550957AC[12], NC_000012.11:g.10550957AC[13], NC_000012.11:g.10550957AC[14], NC_000012.11:g.10550957AC[16], NC_000012.11:g.10550957AC[17], NC_000012.11:g.10550957AC[18], NC_000012.11:g.10550957AC[19], NC_000012.11:g.10550957AC[20], NC_000012.11:g.10550957AC[21], NC_000012.11:g.10550957AC[22], NC_000012.11:g.10550957AC[23], NC_000012.11:g.10550957AC[24], NC_000012.11:g.10550957AC[27], NR_120430.1:n.2682AC[8], NR_120430.1:n.2682AC[9], NR_120430.1:n.2682AC[10], NR_120430.1:n.2682AC[11], NR_120430.1:n.2682AC[12], NR_120430.1:n.2682AC[13], NR_120430.1:n.2682AC[14], NR_120430.1:n.2682AC[16], NR_120430.1:n.2682AC[17], NR_120430.1:n.2682AC[18], NR_120430.1:n.2682AC[19], NR_120430.1:n.2682AC[20], NR_120430.1:n.2682AC[21], NR_120430.1:n.2682AC[22], NR_120430.1:n.2682AC[23], NR_120430.1:n.2682AC[24], NR_120430.1:n.2682AC[27]

    2.

    rs1491139755 has merged into rs3055442 [Homo sapiens]
      Variant type:
      DELINS
      Alleles:
      ACACACACACACAC>-,AC,ACAC,ACACAC,ACACACAC,ACACACACAC,ACACACACACAC,ACACACACACACACAC,ACACACACACACACACAC,ACACACACACACACACACAC,ACACACACACACACACACACAC,ACACACACACACACACACACACAC,ACACACACACACACACACACACACAC,ACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACACACACACAC [Show Flanks]
      Chromosome:
      12:10398374 (GRCh38)
      12:10550973 (GRCh37)
      Canonical SPDI:
      NC_000012.12:10398356:CACACACACACACACACACACACACACACAC:CACACACACACACACAC,NC_000012.12:10398356:CACACACACACACACACACACACACACACAC:CACACACACACACACACAC,NC_000012.12:10398356:CACACACACACACACACACACACACACACAC:CACACACACACACACACACAC,NC_000012.12:10398356:CACACACACACACACACACACACACACACAC:CACACACACACACACACACACAC,NC_000012.12:10398356:CACACACACACACACACACACACACACACAC:CACACACACACACACACACACACAC,NC_000012.12:10398356:CACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACAC,NC_000012.12:10398356:CACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACAC,NC_000012.12:10398356:CACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACAC,NC_000012.12:10398356:CACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACAC,NC_000012.12:10398356:CACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACAC,NC_000012.12:10398356:CACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACAC,NC_000012.12:10398356:CACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACACAC,NC_000012.12:10398356:CACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACACACAC,NC_000012.12:10398356:CACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACACACACAC,NC_000012.12:10398356:CACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACACACACACAC,NC_000012.12:10398356:CACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACACACACACACAC,NC_000012.12:10398356:CACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACACACACACACACACACAC
      Gene:
      KLRC4-KLRK1 (Varview), KLRK1-AS1 (Varview)
      Functional Consequence:
      intron_variant,non_coding_transcript_variant
      Validated:
      by frequency,by alfa,by cluster
      MAF:
      CACACACACACACACACAC=0./0 (ALFA)
      CA=0.4587/2297 (1000Genomes)
      HGVS:
      NC_000012.12:g.10398358AC[8], NC_000012.12:g.10398358AC[9], NC_000012.12:g.10398358AC[10], NC_000012.12:g.10398358AC[11], NC_000012.12:g.10398358AC[12], NC_000012.12:g.10398358AC[13], NC_000012.12:g.10398358AC[14], NC_000012.12:g.10398358AC[16], NC_000012.12:g.10398358AC[17], NC_000012.12:g.10398358AC[18], NC_000012.12:g.10398358AC[19], NC_000012.12:g.10398358AC[20], NC_000012.12:g.10398358AC[21], NC_000012.12:g.10398358AC[22], NC_000012.12:g.10398358AC[23], NC_000012.12:g.10398358AC[24], NC_000012.12:g.10398358AC[27], NC_000012.11:g.10550957AC[8], NC_000012.11:g.10550957AC[9], NC_000012.11:g.10550957AC[10], NC_000012.11:g.10550957AC[11], NC_000012.11:g.10550957AC[12], NC_000012.11:g.10550957AC[13], NC_000012.11:g.10550957AC[14], NC_000012.11:g.10550957AC[16], NC_000012.11:g.10550957AC[17], NC_000012.11:g.10550957AC[18], NC_000012.11:g.10550957AC[19], NC_000012.11:g.10550957AC[20], NC_000012.11:g.10550957AC[21], NC_000012.11:g.10550957AC[22], NC_000012.11:g.10550957AC[23], NC_000012.11:g.10550957AC[24], NC_000012.11:g.10550957AC[27], NR_120430.1:n.2682AC[8], NR_120430.1:n.2682AC[9], NR_120430.1:n.2682AC[10], NR_120430.1:n.2682AC[11], NR_120430.1:n.2682AC[12], NR_120430.1:n.2682AC[13], NR_120430.1:n.2682AC[14], NR_120430.1:n.2682AC[16], NR_120430.1:n.2682AC[17], NR_120430.1:n.2682AC[18], NR_120430.1:n.2682AC[19], NR_120430.1:n.2682AC[20], NR_120430.1:n.2682AC[21], NR_120430.1:n.2682AC[22], NR_120430.1:n.2682AC[23], NR_120430.1:n.2682AC[24], NR_120430.1:n.2682AC[27]

      3.

      rs1490907390 [Homo sapiens]
        Variant type:
        SNV
        Alleles:
        G>A,T [Show Flanks]
        Chromosome:
        12:10396563 (GRCh38)
        12:10549162 (GRCh37)
        Canonical SPDI:
        NC_000012.12:10396562:G:A,NC_000012.12:10396562:G:T
        Gene:
        KLRC4-KLRK1 (Varview), KLRK1-AS1 (Varview)
        Functional Consequence:
        non_coding_transcript_variant,intron_variant
        Validated:
        by frequency,by alfa,by cluster
        MAF:
        T=0./0 (ALFA)
        A=0.000007/1 (GnomAD)
        HGVS:

        4.

        rs1489988099 [Homo sapiens]
          Variant type:
          SNV
          Alleles:
          G>A [Show Flanks]
          Chromosome:
          12:10397837 (GRCh38)
          12:10550436 (GRCh37)
          Canonical SPDI:
          NC_000012.12:10397836:G:A
          Gene:
          KLRC4-KLRK1 (Varview), KLRK1-AS1 (Varview)
          Functional Consequence:
          non_coding_transcript_variant,intron_variant
          Validated:
          by frequency,by alfa,by cluster
          MAF:
          A=0./0 (ALFA)
          A=0.000014/2 (GnomAD)
          A=0.000015/4 (TOPMED)
          HGVS:

          5.

          rs1488555880 [Homo sapiens]
            Variant type:
            DELINS
            Alleles:
            G>- [Show Flanks]
            Chromosome:
            12:10396436 (GRCh38)
            12:10549035 (GRCh37)
            Canonical SPDI:
            NC_000012.12:10396435:GG:G
            Gene:
            KLRC4-KLRK1 (Varview), KLRK1-AS1 (Varview)
            Functional Consequence:
            non_coding_transcript_variant,intron_variant
            Validated:
            by frequency,by alfa,by cluster
            MAF:
            GG=0./0 (ALFA)
            -=0.000007/1 (GnomAD)
            -=0.000015/4 (TOPMED)
            HGVS:

            6.

            rs1486408515 [Homo sapiens]
              Variant type:
              SNV
              Alleles:
              T>C [Show Flanks]
              Chromosome:
              12:10379710 (GRCh38)
              12:10532309 (GRCh37)
              Canonical SPDI:
              NC_000012.12:10379709:T:C
              Gene:
              KLRK1 (Varview), KLRC4-KLRK1 (Varview), KLRK1-AS1 (Varview)
              Functional Consequence:
              non_coding_transcript_variant,coding_sequence_variant,synonymous_variant
              HGVS:

              7.

              rs1484002714 [Homo sapiens]
                Variant type:
                SNV
                Alleles:
                T>C [Show Flanks]
                Chromosome:
                12:10397042 (GRCh38)
                12:10549641 (GRCh37)
                Canonical SPDI:
                NC_000012.12:10397041:T:C
                Gene:
                KLRC4-KLRK1 (Varview), KLRK1-AS1 (Varview)
                Functional Consequence:
                non_coding_transcript_variant,intron_variant
                HGVS:

                8.

                rs1481653070 [Homo sapiens]
                  Variant type:
                  SNV
                  Alleles:
                  C>G,T [Show Flanks]
                  Chromosome:
                  12:10396700 (GRCh38)
                  12:10549299 (GRCh37)
                  Canonical SPDI:
                  NC_000012.12:10396699:C:G,NC_000012.12:10396699:C:T
                  Gene:
                  KLRC4-KLRK1 (Varview), KLRK1-AS1 (Varview)
                  Functional Consequence:
                  intron_variant,non_coding_transcript_variant
                  Validated:
                  by frequency,by alfa,by cluster
                  MAF:
                  T=0./0 (ALFA)
                  T=0.000007/1 (GnomAD)
                  HGVS:

                  9.

                  rs1479737522 [Homo sapiens]
                    Variant type:
                    SNV
                    Alleles:
                    T>G [Show Flanks]
                    Chromosome:
                    12:10396550 (GRCh38)
                    12:10549149 (GRCh37)
                    Canonical SPDI:
                    NC_000012.12:10396549:T:G
                    Gene:
                    KLRC4-KLRK1 (Varview), KLRK1-AS1 (Varview)
                    Functional Consequence:
                    intron_variant,non_coding_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:

                    10.

                    rs1478544221 [Homo sapiens]
                      Variant type:
                      DELINS
                      Alleles:
                      GATTCCTTATAT>- [Show Flanks]
                      Chromosome:
                      12:10363789 (GRCh38)
                      12:10516388 (GRCh37)
                      Canonical SPDI:
                      NC_000012.12:10363787:TGATTCCTTATAT:T
                      Gene:
                      KLRK1-AS1 (Varview)
                      Functional Consequence:
                      non_coding_transcript_variant
                      Validated:
                      by frequency,by alfa
                      MAF:
                      T=0./0 (ALFA)
                      -=0.000004/1 (TOPMED)
                      HGVS:

                      11.

                      rs1478168797 has merged into rs3055442 [Homo sapiens]
                        Variant type:
                        DELINS
                        Alleles:
                        ACACACACACACAC>-,AC,ACAC,ACACAC,ACACACAC,ACACACACAC,ACACACACACAC,ACACACACACACACAC,ACACACACACACACACAC,ACACACACACACACACACAC,ACACACACACACACACACACAC,ACACACACACACACACACACACAC,ACACACACACACACACACACACACAC,ACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACACACACACAC [Show Flanks]
                        Chromosome:
                        12:10398374 (GRCh38)
                        12:10550973 (GRCh37)
                        Canonical SPDI:
                        NC_000012.12:10398356:CACACACACACACACACACACACACACACAC:CACACACACACACACAC,NC_000012.12:10398356:CACACACACACACACACACACACACACACAC:CACACACACACACACACAC,NC_000012.12:10398356:CACACACACACACACACACACACACACACAC:CACACACACACACACACACAC,NC_000012.12:10398356:CACACACACACACACACACACACACACACAC:CACACACACACACACACACACAC,NC_000012.12:10398356:CACACACACACACACACACACACACACACAC:CACACACACACACACACACACACAC,NC_000012.12:10398356:CACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACAC,NC_000012.12:10398356:CACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACAC,NC_000012.12:10398356:CACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACAC,NC_000012.12:10398356:CACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACAC,NC_000012.12:10398356:CACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACAC,NC_000012.12:10398356:CACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACAC,NC_000012.12:10398356:CACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACACAC,NC_000012.12:10398356:CACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACACACAC,NC_000012.12:10398356:CACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACACACACAC,NC_000012.12:10398356:CACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACACACACACAC,NC_000012.12:10398356:CACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACACACACACACAC,NC_000012.12:10398356:CACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACACACACACACACACACAC
                        Gene:
                        KLRC4-KLRK1 (Varview), KLRK1-AS1 (Varview)
                        Functional Consequence:
                        intron_variant,non_coding_transcript_variant
                        Validated:
                        by frequency,by alfa,by cluster
                        MAF:
                        CACACACACACACACACAC=0./0 (ALFA)
                        CA=0.4587/2297 (1000Genomes)
                        HGVS:
                        NC_000012.12:g.10398358AC[8], NC_000012.12:g.10398358AC[9], NC_000012.12:g.10398358AC[10], NC_000012.12:g.10398358AC[11], NC_000012.12:g.10398358AC[12], NC_000012.12:g.10398358AC[13], NC_000012.12:g.10398358AC[14], NC_000012.12:g.10398358AC[16], NC_000012.12:g.10398358AC[17], NC_000012.12:g.10398358AC[18], NC_000012.12:g.10398358AC[19], NC_000012.12:g.10398358AC[20], NC_000012.12:g.10398358AC[21], NC_000012.12:g.10398358AC[22], NC_000012.12:g.10398358AC[23], NC_000012.12:g.10398358AC[24], NC_000012.12:g.10398358AC[27], NC_000012.11:g.10550957AC[8], NC_000012.11:g.10550957AC[9], NC_000012.11:g.10550957AC[10], NC_000012.11:g.10550957AC[11], NC_000012.11:g.10550957AC[12], NC_000012.11:g.10550957AC[13], NC_000012.11:g.10550957AC[14], NC_000012.11:g.10550957AC[16], NC_000012.11:g.10550957AC[17], NC_000012.11:g.10550957AC[18], NC_000012.11:g.10550957AC[19], NC_000012.11:g.10550957AC[20], NC_000012.11:g.10550957AC[21], NC_000012.11:g.10550957AC[22], NC_000012.11:g.10550957AC[23], NC_000012.11:g.10550957AC[24], NC_000012.11:g.10550957AC[27], NR_120430.1:n.2682AC[8], NR_120430.1:n.2682AC[9], NR_120430.1:n.2682AC[10], NR_120430.1:n.2682AC[11], NR_120430.1:n.2682AC[12], NR_120430.1:n.2682AC[13], NR_120430.1:n.2682AC[14], NR_120430.1:n.2682AC[16], NR_120430.1:n.2682AC[17], NR_120430.1:n.2682AC[18], NR_120430.1:n.2682AC[19], NR_120430.1:n.2682AC[20], NR_120430.1:n.2682AC[21], NR_120430.1:n.2682AC[22], NR_120430.1:n.2682AC[23], NR_120430.1:n.2682AC[24], NR_120430.1:n.2682AC[27]

                        12.

                        rs1476429775 [Homo sapiens]
                          Variant type:
                          SNV
                          Alleles:
                          A>G [Show Flanks]
                          Chromosome:
                          12:10397863 (GRCh38)
                          12:10550462 (GRCh37)
                          Canonical SPDI:
                          NC_000012.12:10397862:A:G
                          Gene:
                          KLRC4-KLRK1 (Varview), KLRK1-AS1 (Varview)
                          Functional Consequence:
                          intron_variant,non_coding_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:

                          13.

                          rs1473494765 [Homo sapiens]
                            Variant type:
                            SNV
                            Alleles:
                            G>A [Show Flanks]
                            Chromosome:
                            12:10397059 (GRCh38)
                            12:10549658 (GRCh37)
                            Canonical SPDI:
                            NC_000012.12:10397058:G:A
                            Gene:
                            KLRC4-KLRK1 (Varview), KLRK1-AS1 (Varview)
                            Functional Consequence:
                            intron_variant,non_coding_transcript_variant
                            Validated:
                            by frequency,by alfa
                            MAF:
                            A=0./0 (ALFA)
                            A=0.000004/1 (TOPMED)
                            HGVS:

                            14.

                            rs1473484323 [Homo sapiens]
                              Variant type:
                              SNV
                              Alleles:
                              C>T [Show Flanks]
                              Chromosome:
                              12:10398326 (GRCh38)
                              12:10550925 (GRCh37)
                              Canonical SPDI:
                              NC_000012.12:10398325:C:T
                              Gene:
                              KLRC4-KLRK1 (Varview), KLRK1-AS1 (Varview)
                              Functional Consequence:
                              intron_variant,non_coding_transcript_variant
                              Validated:
                              by frequency,by alfa,by cluster
                              MAF:
                              T=0./0 (ALFA)
                              T=0.000007/1 (GnomAD)
                              T=0.000008/2 (TOPMED)
                              HGVS:

                              15.

                              rs1471622372 [Homo sapiens]
                                Variant type:
                                DEL
                                Alleles:
                                ATG>- [Show Flanks]
                                Chromosome:
                                12:10396368 (GRCh38)
                                12:10548967 (GRCh37)
                                Canonical SPDI:
                                NC_000012.12:10396367:ATG:
                                Gene:
                                KLRC4-KLRK1 (Varview), KLRK1-AS1 (Varview)
                                Functional Consequence:
                                intron_variant,non_coding_transcript_variant
                                Validated:
                                by frequency,by alfa
                                MAF:
                                -=0./0 (ALFA)
                                -=0.000004/1 (TOPMED)
                                HGVS:

                                16.

                                rs1470260319 [Homo sapiens]
                                  Variant type:
                                  SNV
                                  Alleles:
                                  C>A,G,T [Show Flanks]
                                  Chromosome:
                                  12:10396250 (GRCh38)
                                  12:10548849 (GRCh37)
                                  Canonical SPDI:
                                  NC_000012.12:10396249:C:A,NC_000012.12:10396249:C:G,NC_000012.12:10396249:C:T
                                  Gene:
                                  KLRC4-KLRK1 (Varview), KLRK1-AS1 (Varview)
                                  Functional Consequence:
                                  intron_variant,non_coding_transcript_variant
                                  Validated:
                                  by frequency,by alfa,by cluster
                                  MAF:
                                  G=0./0 (ALFA)
                                  T=0.000007/1 (GnomAD)
                                  HGVS:

                                  17.

                                  rs1468693250 [Homo sapiens]
                                    Variant type:
                                    SNV
                                    Alleles:
                                    A>G [Show Flanks]
                                    Chromosome:
                                    12:10397850 (GRCh38)
                                    12:10550449 (GRCh37)
                                    Canonical SPDI:
                                    NC_000012.12:10397849:A:G
                                    Gene:
                                    KLRC4-KLRK1 (Varview), KLRK1-AS1 (Varview)
                                    Functional Consequence:
                                    intron_variant,non_coding_transcript_variant
                                    Validated:
                                    by frequency,by alfa,by cluster
                                    MAF:
                                    G=0./0 (ALFA)
                                    G=0.000011/3 (TOPMED)
                                    G=0.000029/4 (GnomAD)
                                    HGVS:

                                    18.

                                    rs1468511980 [Homo sapiens]
                                      Variant type:
                                      SNV
                                      Alleles:
                                      A>T [Show Flanks]
                                      Chromosome:
                                      12:10379708 (GRCh38)
                                      12:10532307 (GRCh37)
                                      Canonical SPDI:
                                      NC_000012.12:10379707:A:T
                                      Gene:
                                      KLRK1 (Varview), KLRC4-KLRK1 (Varview), KLRK1-AS1 (Varview)
                                      Functional Consequence:
                                      coding_sequence_variant,missense_variant,non_coding_transcript_variant
                                      Validated:
                                      by frequency,by alfa,by cluster
                                      MAF:
                                      T=0./0 (ALFA)
                                      T=0.000004/1 (TOPMED)
                                      T=0.000007/1 (GnomAD)
                                      HGVS:

                                      19.

                                      rs1465379629 [Homo sapiens]
                                        Variant type:
                                        SNV
                                        Alleles:
                                        T>A [Show Flanks]
                                        Chromosome:
                                        12:10397744 (GRCh38)
                                        12:10550343 (GRCh37)
                                        Canonical SPDI:
                                        NC_000012.12:10397743:T:A
                                        Gene:
                                        KLRC4-KLRK1 (Varview), KLRK1-AS1 (Varview)
                                        Functional Consequence:
                                        intron_variant,non_coding_transcript_variant
                                        Validated:
                                        by frequency,by alfa
                                        MAF:
                                        A=0./0 (ALFA)
                                        A=0.000046/5 (GnomAD)
                                        HGVS:

                                        20.

                                        rs1464357498 [Homo sapiens]
                                          Variant type:
                                          SNV
                                          Alleles:
                                          G>A [Show Flanks]
                                          Chromosome:
                                          12:10379786 (GRCh38)
                                          12:10532385 (GRCh37)
                                          Canonical SPDI:
                                          NC_000012.12:10379785:G:A
                                          Gene:
                                          KLRK1 (Varview), KLRC4-KLRK1 (Varview), KLRK1-AS1 (Varview)
                                          Functional Consequence:
                                          coding_sequence_variant,missense_variant,non_coding_transcript_variant
                                          Validated:
                                          by frequency
                                          MAF:
                                          A=0.000004/1 (GnomAD_exomes)
                                          HGVS:

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