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1.

rs1491510062 has merged into rs56158505 [Homo sapiens]
    Variant type:
    DELINS
    Alleles:
    ACACACACACAC>-,AC,ACAC,ACACAC,ACACACAC,ACACACACAC,ACACACACACACAC,ACACACACACACACAC,ACACACACACACACACAC,ACACACACACACACACACAC,ACACACACACACACACACACAC,ACACACACACACACACACACACAC,ACACACACACACACACACACACACAC,ACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACACACACAC [Show Flanks]
    Chromosome:
    X:46505784 (GRCh38)
    X:46365219 (GRCh37)
    Canonical SPDI:
    NC_000023.11:46505768:CACACACACACACACACACACACACAC:CACACACACACACAC,NC_000023.11:46505768:CACACACACACACACACACACACACAC:CACACACACACACACAC,NC_000023.11:46505768:CACACACACACACACACACACACACAC:CACACACACACACACACAC,NC_000023.11:46505768:CACACACACACACACACACACACACAC:CACACACACACACACACACAC,NC_000023.11:46505768:CACACACACACACACACACACACACAC:CACACACACACACACACACACAC,NC_000023.11:46505768:CACACACACACACACACACACACACAC:CACACACACACACACACACACACAC,NC_000023.11:46505768:CACACACACACACACACACACACACAC:CACACACACACACACACACACACACACAC,NC_000023.11:46505768:CACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACAC,NC_000023.11:46505768:CACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACAC,NC_000023.11:46505768:CACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACAC,NC_000023.11:46505768:CACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACAC,NC_000023.11:46505768:CACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACAC,NC_000023.11:46505768:CACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACACAC,NC_000023.11:46505768:CACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACACACAC,NC_000023.11:46505768:CACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACACACACAC,NC_000023.11:46505768:CACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACACACACACAC,NC_000023.11:46505768:CACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACACACACACACAC,NC_000023.11:46505768:CACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACACACACACACACAC
    Gene:
    ZNF674 (Varview)
    Functional Consequence:
    intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    CACACACACACACACAC=0./0 (ALFA)
    -=0.000042/11 (TOPMED)
    -=0.009801/37 (1000Genomes)
    HGVS:
    NC_000023.11:g.46505770AC[7], NC_000023.11:g.46505770AC[8], NC_000023.11:g.46505770AC[9], NC_000023.11:g.46505770AC[10], NC_000023.11:g.46505770AC[11], NC_000023.11:g.46505770AC[12], NC_000023.11:g.46505770AC[14], NC_000023.11:g.46505770AC[15], NC_000023.11:g.46505770AC[16], NC_000023.11:g.46505770AC[17], NC_000023.11:g.46505770AC[18], NC_000023.11:g.46505770AC[19], NC_000023.11:g.46505770AC[20], NC_000023.11:g.46505770AC[21], NC_000023.11:g.46505770AC[22], NC_000023.11:g.46505770AC[23], NC_000023.11:g.46505770AC[24], NC_000023.11:g.46505770AC[25], NC_000023.10:g.46365205AC[7], NC_000023.10:g.46365205AC[8], NC_000023.10:g.46365205AC[9], NC_000023.10:g.46365205AC[10], NC_000023.10:g.46365205AC[11], NC_000023.10:g.46365205AC[12], NC_000023.10:g.46365205AC[14], NC_000023.10:g.46365205AC[15], NC_000023.10:g.46365205AC[16], NC_000023.10:g.46365205AC[17], NC_000023.10:g.46365205AC[18], NC_000023.10:g.46365205AC[19], NC_000023.10:g.46365205AC[20], NC_000023.10:g.46365205AC[21], NC_000023.10:g.46365205AC[22], NC_000023.10:g.46365205AC[23], NC_000023.10:g.46365205AC[24], NC_000023.10:g.46365205AC[25], NG_023376.2:g.44664TG[7], NG_023376.2:g.44664TG[8], NG_023376.2:g.44664TG[9], NG_023376.2:g.44664TG[10], NG_023376.2:g.44664TG[11], NG_023376.2:g.44664TG[12], NG_023376.2:g.44664TG[14], NG_023376.2:g.44664TG[15], NG_023376.2:g.44664TG[16], NG_023376.2:g.44664TG[17], NG_023376.2:g.44664TG[18], NG_023376.2:g.44664TG[19], NG_023376.2:g.44664TG[20], NG_023376.2:g.44664TG[21], NG_023376.2:g.44664TG[22], NG_023376.2:g.44664TG[23], NG_023376.2:g.44664TG[24], NG_023376.2:g.44664TG[25]

    2.

    rs1491500947 has merged into rs749919543 [Homo sapiens]
      Variant type:
      DELINS
      Alleles:
      GA>-,GAAAGA [Show Flanks]
      Chromosome:
      X:46519253 (GRCh38)
      X:46378688 (GRCh37)
      Canonical SPDI:
      NC_000023.11:46519251:AGA:A,NC_000023.11:46519251:AGA:AGAAAGA
      Gene:
      ZNF674 (Varview)
      Functional Consequence:
      intron_variant
      Validated:
      by frequency,by alfa,by cluster
      MAF:
      A=0./0 (ALFA)
      AGAA=0.05434/157 (ALSPAC)
      AGAA=0.05852/217 (TWINSUK)
      HGVS:

      3.

      rs1491487978 [Homo sapiens]
        Variant type:
        DEL
        Alleles:
        CA>- [Show Flanks]
        Chromosome:
        X:46502305 (GRCh38)
        X:46361740 (GRCh37)
        Canonical SPDI:
        NC_000023.11:46502304:CA:
        Gene:
        ZNF674 (Varview)
        Functional Consequence:
        intron_variant
        Validated:
        by frequency,by alfa
        MAF:
        -=0.00008/1 (ALFA)
        HGVS:

        4.

        rs1491463035 [Homo sapiens]
          Variant type:
          DELINS
          Alleles:
          ->A,AA [Show Flanks]
          Chromosome:
          X:46541359 (GRCh38)
          X:46400795 (GRCh37)
          Canonical SPDI:
          NC_000023.11:46541359:A:AA,NC_000023.11:46541359:A:AAA
          Gene:
          ZNF674 (Varview)
          Functional Consequence:
          intron_variant
          Validated:
          by frequency,by alfa
          MAF:
          AAA=0./0 (ALFA)
          A=0.00039/5 (TOMMO)
          HGVS:

          5.

          rs1491435892 [Homo sapiens]
            Variant type:
            DELINS
            Alleles:
            ->GGATAGATAGAT [Show Flanks]
            Chromosome:
            X:46519252 (GRCh38)
            X:46378688 (GRCh37)
            Canonical SPDI:
            NC_000023.11:46519252:GATAGATAGAT:GATAGATAGATGGATAGATAGAT
            Gene:
            ZNF674 (Varview)
            Functional Consequence:
            intron_variant
            Validated:
            by frequency,by alfa
            MAF:
            GATAGATAGATGGATAGATAGAT=0./0 (ALFA)
            HGVS:

            6.

            rs1491413252 [Homo sapiens]
              Variant type:
              DELINS
              Alleles:
              ->GG [Show Flanks]
              Chromosome:
              X:46501663 (GRCh38)
              X:46361099 (GRCh37)
              Canonical SPDI:
              NC_000023.11:46501663:G:GGG
              Gene:
              ZNF674 (Varview)
              Functional Consequence:
              intron_variant
              HGVS:

              7.

              rs1491404270 has merged into rs372308686 [Homo sapiens]
                Variant type:
                DELINS
                Alleles:
                GTGTGTGT>-,GT,GTGT,GTGTGT,GTGTGTGTGT,GTGTGTGTGTGT,GTGTGTGTGTGTGT,GTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGT [Show Flanks]
                Chromosome:
                X:46501680 (GRCh38)
                X:46361115 (GRCh37)
                Canonical SPDI:
                NC_000023.11:46501662:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGT,NC_000023.11:46501662:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGT,NC_000023.11:46501662:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGT,NC_000023.11:46501662:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGT,NC_000023.11:46501662:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000023.11:46501662:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000023.11:46501662:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000023.11:46501662:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000023.11:46501662:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000023.11:46501662:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000023.11:46501662:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000023.11:46501662:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000023.11:46501662:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000023.11:46501662:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT
                Gene:
                ZNF674 (Varview)
                Functional Consequence:
                intron_variant
                Validated:
                by frequency,by alfa,by cluster
                MAF:
                TGTGTGTGTGTGTGTGTGT=0./0 (ALFA)
                TG=0.2/8 (GENOME_DK)
                HGVS:
                NC_000023.11:g.46501664GT[8], NC_000023.11:g.46501664GT[9], NC_000023.11:g.46501664GT[10], NC_000023.11:g.46501664GT[11], NC_000023.11:g.46501664GT[13], NC_000023.11:g.46501664GT[14], NC_000023.11:g.46501664GT[15], NC_000023.11:g.46501664GT[16], NC_000023.11:g.46501664GT[17], NC_000023.11:g.46501664GT[18], NC_000023.11:g.46501664GT[19], NC_000023.11:g.46501664GT[20], NC_000023.11:g.46501664GT[21], NC_000023.11:g.46501664GT[22], NC_000023.10:g.46361099GT[8], NC_000023.10:g.46361099GT[9], NC_000023.10:g.46361099GT[10], NC_000023.10:g.46361099GT[11], NC_000023.10:g.46361099GT[13], NC_000023.10:g.46361099GT[14], NC_000023.10:g.46361099GT[15], NC_000023.10:g.46361099GT[16], NC_000023.10:g.46361099GT[17], NC_000023.10:g.46361099GT[18], NC_000023.10:g.46361099GT[19], NC_000023.10:g.46361099GT[20], NC_000023.10:g.46361099GT[21], NC_000023.10:g.46361099GT[22], NG_023376.2:g.48772CA[8], NG_023376.2:g.48772CA[9], NG_023376.2:g.48772CA[10], NG_023376.2:g.48772CA[11], NG_023376.2:g.48772CA[13], NG_023376.2:g.48772CA[14], NG_023376.2:g.48772CA[15], NG_023376.2:g.48772CA[16], NG_023376.2:g.48772CA[17], NG_023376.2:g.48772CA[18], NG_023376.2:g.48772CA[19], NG_023376.2:g.48772CA[20], NG_023376.2:g.48772CA[21], NG_023376.2:g.48772CA[22]

                8.

                rs1491371711 [Homo sapiens]
                  Variant type:
                  DEL
                  Alleles:
                  CG>- [Show Flanks]
                  Chromosome:
                  X:46505795 (GRCh38)
                  X:46365230 (GRCh37)
                  Canonical SPDI:
                  NC_000023.11:46505794:CG:
                  Gene:
                  ZNF674 (Varview)
                  Functional Consequence:
                  intron_variant
                  Validated:
                  by frequency,by alfa
                  MAF:
                  -=0./0 (ALFA)
                  HGVS:

                  9.

                  rs1491330854 has merged into rs376743250 [Homo sapiens]
                    Variant type:
                    DELINS
                    Alleles:
                    AA>-,A [Show Flanks]
                    Chromosome:
                    X:46519265 (GRCh38)
                    X:46378700 (GRCh37)
                    Canonical SPDI:
                    NC_000023.11:46519263:AAA:A,NC_000023.11:46519263:AAA:AA
                    Gene:
                    ZNF674 (Varview)
                    Functional Consequence:
                    intron_variant
                    Validated:
                    by frequency,by alfa,by cluster
                    MAF:
                    A=0./0 (ALFA)
                    -=0.2762/1024 (TWINSUK)
                    -=0.3022/873 (ALSPAC)
                    HGVS:

                    10.

                    rs1491304429 [Homo sapiens]
                      Variant type:
                      DELINS
                      Alleles:
                      CA>- [Show Flanks]
                      Chromosome:
                      X:46541361 (GRCh38)
                      X:46400796 (GRCh37)
                      Canonical SPDI:
                      NC_000023.11:46541358:CACA:CA
                      Gene:
                      ZNF674 (Varview)
                      Functional Consequence:
                      intron_variant
                      Validated:
                      by frequency,by alfa
                      MAF:
                      CACA=0./0 (ALFA)
                      HGVS:

                      11.

                      rs1491247337 [Homo sapiens]
                        Variant type:
                        DEL
                        Alleles:
                        TA>- [Show Flanks]
                        Chromosome:
                        X:46498722 (GRCh38)
                        X:46358157 (GRCh37)
                        Canonical SPDI:
                        NC_000023.11:46498721:TA:
                        Gene:
                        ZNF674 (Varview)
                        Functional Consequence:
                        3_prime_UTR_variant
                        Clinical significance:
                        uncertain-significance
                        Validated:
                        by frequency,by alfa,by cluster
                        MAF:
                        -=0.20575/3243 (ALFA)
                        -=0.07465/933 (TOMMO)
                        -=0.24741/19004 (GnomAD)
                        HGVS:

                        12.

                        rs1491244138 [Homo sapiens]
                          Variant type:
                          DEL
                          Alleles:
                          CT>- [Show Flanks]
                          Chromosome:
                          X:46498721 (GRCh38)
                          X:46358156 (GRCh37)
                          Canonical SPDI:
                          NC_000023.11:46498720:CT:
                          Gene:
                          ZNF674 (Varview)
                          Functional Consequence:
                          3_prime_UTR_variant
                          Validated:
                          by frequency,by alfa,by cluster
                          MAF:
                          -=0.00649/77 (ALFA)
                          -=0.00018/2 (TOMMO)
                          HGVS:

                          13.

                          rs1491042548 [Homo sapiens]
                            Variant type:
                            DELINS
                            Alleles:
                            A>-,AA [Show Flanks]
                            Chromosome:
                            X:46532480 (GRCh38)
                            X:46391915 (GRCh37)
                            Canonical SPDI:
                            NC_000023.11:46532479:AAAAAA:AAAAA,NC_000023.11:46532479:AAAAAA:AAAAAAA
                            Gene:
                            ZNF674 (Varview)
                            Functional Consequence:
                            intron_variant
                            Validated:
                            by frequency,by alfa,by cluster
                            MAF:
                            AAAAAAA=0./0 (ALFA)
                            -=0.00021/1 (1000Genomes)
                            HGVS:

                            14.

                            rs1490899965 [Homo sapiens]
                              Variant type:
                              SNV
                              Alleles:
                              G>A [Show Flanks]
                              Chromosome:
                              X:46508371 (GRCh38)
                              X:46367806 (GRCh37)
                              Canonical SPDI:
                              NC_000023.11:46508370:G:A
                              Gene:
                              ZNF674 (Varview)
                              Functional Consequence:
                              intron_variant
                              Validated:
                              by frequency,by alfa
                              MAF:
                              A=0.00012/2 (ALFA)
                              HGVS:

                              15.

                              rs1490828187 [Homo sapiens]
                                Variant type:
                                SNV
                                Alleles:
                                G>T [Show Flanks]
                                Chromosome:
                                X:46529640 (GRCh38)
                                X:46389075 (GRCh37)
                                Canonical SPDI:
                                NC_000023.11:46529639:G:T
                                Gene:
                                ZNF674 (Varview)
                                Functional Consequence:
                                intron_variant
                                Validated:
                                by frequency,by alfa,by cluster
                                MAF:
                                T=0./0 (ALFA)
                                T=0.000015/4 (TOPMED)
                                T=0.000031/3 (GnomAD)
                                HGVS:

                                16.

                                rs1490705665 [Homo sapiens]
                                  Variant type:
                                  DELINS
                                  Alleles:
                                  A>- [Show Flanks]
                                  Chromosome:
                                  X:46525304 (GRCh38)
                                  X:46384739 (GRCh37)
                                  Canonical SPDI:
                                  NC_000023.11:46525303:AAAAAA:AAAAA
                                  Gene:
                                  ZNF674 (Varview)
                                  Functional Consequence:
                                  intron_variant
                                  Validated:
                                  by frequency,by alfa,by cluster
                                  MAF:
                                  AAAAA=0./0 (ALFA)
                                  -=0.000004/1 (TOPMED)
                                  HGVS:

                                  17.

                                  rs1490657804 [Homo sapiens]
                                    Variant type:
                                    SNV
                                    Alleles:
                                    G>A [Show Flanks]
                                    Chromosome:
                                    X:46531165 (GRCh38)
                                    X:46390600 (GRCh37)
                                    Canonical SPDI:
                                    NC_000023.11:46531164:G:A
                                    Gene:
                                    ZNF674 (Varview)
                                    Functional Consequence:
                                    intron_variant
                                    Validated:
                                    by frequency,by alfa,by cluster
                                    MAF:
                                    A=0.000071/1 (ALFA)
                                    A=0.000114/12 (GnomAD)
                                    A=0.000298/79 (TOPMED)
                                    HGVS:

                                    18.

                                    rs1490579036 [Homo sapiens]
                                      Variant type:
                                      SNV
                                      Alleles:
                                      C>T [Show Flanks]
                                      Chromosome:
                                      X:46538080 (GRCh38)
                                      X:46397515 (GRCh37)
                                      Canonical SPDI:
                                      NC_000023.11:46538079:C:T
                                      Gene:
                                      ZNF674 (Varview)
                                      Functional Consequence:
                                      intron_variant
                                      Validated:
                                      by frequency,by alfa,by cluster
                                      MAF:
                                      T=0./0 (ALFA)
                                      T=0.000008/2 (TOPMED)
                                      T=0.000033/3 (GnomAD)
                                      HGVS:

                                      19.

                                      rs1490549348 [Homo sapiens]
                                        Variant type:
                                        SNV
                                        Alleles:
                                        C>T [Show Flanks]
                                        Chromosome:
                                        X:46536721 (GRCh38)
                                        X:46396156 (GRCh37)
                                        Canonical SPDI:
                                        NC_000023.11:46536720:C:T
                                        Gene:
                                        ZNF674 (Varview)
                                        Functional Consequence:
                                        intron_variant
                                        Validated:
                                        by frequency,by alfa,by cluster
                                        MAF:
                                        T=0./0 (ALFA)
                                        T=0.000008/2 (TOPMED)
                                        T=0.00001/1 (GnomAD)
                                        T=0.000046/1 (TOMMO)
                                        HGVS:

                                        20.

                                        rs1490525550 [Homo sapiens]
                                          Variant type:
                                          DEL
                                          Alleles:
                                          C>- [Show Flanks]
                                          Chromosome:
                                          X:46533855 (GRCh38)
                                          X:46393290 (GRCh37)
                                          Canonical SPDI:
                                          NC_000023.11:46533854:C:
                                          Gene:
                                          ZNF674 (Varview)
                                          Functional Consequence:
                                          intron_variant
                                          HGVS:

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