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Items: 1 to 20 of 14630

1.

rs1491538601 [Homo sapiens]
    Variant type:
    DELINS
    Alleles:
    ->GT [Show Flanks]
    Chromosome:
    16:47115715 (GRCh38)
    16:47149627 (GRCh37)
    Canonical SPDI:
    NC_000016.10:47115715:T:TGT
    Gene:
    NETO2 (Varview)
    Functional Consequence:
    intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    TGT=0.000124/2 (ALFA)
    TG=0.000071/1 (TOMMO)
    TG=0.000314/35 (GnomAD)
    HGVS:

    2.

    rs1491398947 has merged into rs918750034 [Homo sapiens]
      Variant type:
      DELINS
      Alleles:
      TATATA>-,TA,TATA,TATATATA,TATATATACATGTATATATATATACATATATATATATATATATA,TATATATATA,TATATATATACATGTATATATATATACATATATATATATATATATA,TATATATATATA,TATATATATATATA,TATATATATATATATA,TATATATATATATATATATA,TATATATATATATATATATATATATA,TATATATATATATATATATATATATATA,TATATATATATATATATGTATATATATATATATATA,TATATATATATATATATGTATATATATATATATATATATATA,TATATATATATATATGTATATATATATATATATA,TATATATATATATATGTATATATATATATATATATATATA,TATATATATATATATGTATATATATATATATATATATATATA,TATATATATATATATGTATATATATATATATATATATATATATA,TATATATATATATATGTATATATATATATATATATATATATATATA,TATATATATATATGTATAGATATATATATATATATATA,TATATATATATATGTATATATATATATATATATATA,TATATATATATATGTATATATATATATATATATATATA,TATATATATATATGTATATATATATATATATATATATATA,TATATATATATATGTATATATATATATATATATATATATATA,TATATATATATATGTATATATATATATATATATATATATATATA,TATATATATATATGTATATATATATATATATATATATATATATATA,TATATATATATATGTATATATATATATATATATATATGTATATATATATATATATATATATA,TATATATATATATGTATATATATATATATATATATGTGTATATATATATATATATATATA,TATATATATATATGTGTATATATATATATATATA,TATATATATATATGTGTATATATATATATATATATATA,TATATATATATGTATATATATATATATATATATA,TATATATATATGTATATATATATATATATATATATA,TATATATATATGTATATATATATATATATATATATGTATATATATATATATATATATA,TATATATATATGTATATATATATATATATATATGTATATATATATATATATATATA,TATATATATATGTATATATATATATATATATATGTGTATATATATATATATATATA,TATATATATGTATATATATATATATATATATGTATATATATATATATATATATA,TATATATGTATATATATATATATATATATATA,TATATATGTATATATATATATATATATATATGTATATATATATATATATATATATA,TATATATGTGTATATATATATATATATATATA [Show Flanks]
      Chromosome:
      16:47115726 (GRCh38)
      16:47149637 (GRCh37)
      Canonical SPDI:
      NC_000016.10:47115714:ATATATATATATATATA:ATATATATATA,NC_000016.10:47115714:ATATATATATATATATA:ATATATATATATA,NC_000016.10:47115714:ATATATATATATATATA:ATATATATATATATA,NC_000016.10:47115714:ATATATATATATATATA:ATATATATATATATATATA,NC_000016.10:47115714:ATATATATATATATATA:ATATATATATATATATATACATGTATATATATATACATATATATATATATATATA,NC_000016.10:47115714:ATATATATATATATATA:ATATATATATATATATATATA,NC_000016.10:47115714:ATATATATATATATATA:ATATATATATATATATATATACATGTATATATATATACATATATATATATATATATA,NC_000016.10:47115714:ATATATATATATATATA:ATATATATATATATATATATATA,NC_000016.10:47115714:ATATATATATATATATA:ATATATATATATATATATATATATA,NC_000016.10:47115714:ATATATATATATATATA:ATATATATATATATATATATATATATA,NC_000016.10:47115714:ATATATATATATATATA:ATATATATATATATATATATATATATATATA,NC_000016.10:47115714:ATATATATATATATATA:ATATATATATATATATATATATATATATATATATATA,NC_000016.10:47115714:ATATATATATATATATA:ATATATATATATATATATATATATATATATATATATATA,NC_000016.10:47115714:ATATATATATATATATA:ATATATATATATATATATATATATATATGTATATATATATATATATA,NC_000016.10:47115714:ATATATATATATATATA:ATATATATATATATATATATATATATATGTATATATATATATATATATATATA,NC_000016.10:47115714:ATATATATATATATATA:ATATATATATATATATATATATATATGTATATATATATATATATA,NC_000016.10:47115714:ATATATATATATATATA:ATATATATATATATATATATATATATGTATATATATATATATATATATATA,NC_000016.10:47115714:ATATATATATATATATA:ATATATATATATATATATATATATATGTATATATATATATATATATATATATA,NC_000016.10:47115714:ATATATATATATATATA:ATATATATATATATATATATATATATGTATATATATATATATATATATATATATA,NC_000016.10:47115714:ATATATATATATATATA:ATATATATATATATATATATATATATGTATATATATATATATATATATATATATATA,NC_000016.10:47115714:ATATATATATATATATA:ATATATATATATATATATATATATGTATAGATATATATATATATATATA,NC_000016.10:47115714:ATATATATATATATATA:ATATATATATATATATATATATATGTATATATATATATATATATATA,NC_000016.10:47115714:ATATATATATATATATA:ATATATATATATATATATATATATGTATATATATATATATATATATATA,NC_000016.10:47115714:ATATATATATATATATA:ATATATATATATATATATATATATGTATATATATATATATATATATATATA,NC_000016.10:47115714:ATATATATATATATATA:ATATATATATATATATATATATATGTATATATATATATATATATATATATATA,NC_000016.10:47115714:ATATATATATATATATA:ATATATATATATATATATATATATGTATATATATATATATATATATATATATATA,NC_000016.10:47115714:ATATATATATATATATA:ATATATATATATATATATATATATGTATATATATATATATATATATATATATATATA,NC_000016.10:47115714:ATATATATATATATATA:ATATATATATATATATATATATATGTATATATATATATATATATATATGTATATATATATATATATATATATA,NC_000016.10:47115714:ATATATATATATATATA:ATATATATATATATATATATATATGTATATATATATATATATATATGTGTATATATATATATATATATATA,NC_000016.10:47115714:ATATATATATATATATA:ATATATATATATATATATATATATGTGTATATATATATATATATA,NC_000016.10:47115714:ATATATATATATATATA:ATATATATATATATATATATATATGTGTATATATATATATATATATATA,NC_000016.10:47115714:ATATATATATATATATA:ATATATATATATATATATATATGTATATATATATATATATATATA,NC_000016.10:47115714:ATATATATATATATATA:ATATATATATATATATATATATGTATATATATATATATATATATATA,NC_000016.10:47115714:ATATATATATATATATA:ATATATATATATATATATATATGTATATATATATATATATATATATGTATATATATATATATATATATA,NC_000016.10:47115714:ATATATATATATATATA:ATATATATATATATATATATATGTATATATATATATATATATATGTATATATATATATATATATATA,NC_000016.10:47115714:ATATATATATATATATA:ATATATATATATATATATATATGTATATATATATATATATATATGTGTATATATATATATATATATA,NC_000016.10:47115714:ATATATATATATATATA:ATATATATATATATATATATGTATATATATATATATATATATGTATATATATATATATATATATA,NC_000016.10:47115714:ATATATATATATATATA:ATATATATATATATATATGTATATATATATATATATATATATA,NC_000016.10:47115714:ATATATATATATATATA:ATATATATATATATATATGTATATATATATATATATATATATGTATATATATATATATATATATATA,NC_000016.10:47115714:ATATATATATATATATA:ATATATATATATATATATGTGTATATATATATATATATATATA
      Gene:
      NETO2 (Varview)
      Functional Consequence:
      intron_variant
      Validated:
      by frequency,by alfa,by cluster
      MAF:
      ATATATATATATA=0./0 (ALFA)
      HGVS:
      NC_000016.10:g.47115716TA[5], NC_000016.10:g.47115716TA[6], NC_000016.10:g.47115716TA[7], NC_000016.10:g.47115716TA[9], NC_000016.10:g.47115715_47115731AT[9]ACATGTATATATATATACATATATATATATATATATA[1], NC_000016.10:g.47115716TA[10], NC_000016.10:g.47115715_47115731AT[10]ACATGTATATATATATACATATATATATATATATATA[1], NC_000016.10:g.47115716TA[11], NC_000016.10:g.47115716TA[12], NC_000016.10:g.47115716TA[13], NC_000016.10:g.47115716TA[15], NC_000016.10:g.47115716TA[18], NC_000016.10:g.47115716TA[19], NC_000016.10:g.47115715_47115731AT[14]GTATATATATATATATATA[1], NC_000016.10:g.47115715_47115731AT[14]GTATATATATATATATATATATATA[1], NC_000016.10:g.47115715_47115731AT[13]GTATATATATATATATATA[1], NC_000016.10:g.47115715_47115731AT[13]GTATATATATATATATATATATATA[1], NC_000016.10:g.47115715_47115731AT[13]GTATATATATATATATATATATATATA[1], NC_000016.10:g.47115715_47115731AT[13]GTATATATATATATATATATATATATATA[1], NC_000016.10:g.47115715_47115731AT[13]GTATATATATATATATATATATATATATATA[1], NC_000016.10:g.47115715_47115731AT[12]GTATAGATATATATATATATATATA[1], NC_000016.10:g.47115715_47115731AT[12]GTATATATATATATATATATATA[1], NC_000016.10:g.47115715_47115731AT[12]GTATATATATATATATATATATATA[1], NC_000016.10:g.47115715_47115731AT[12]GTATATATATATATATATATATATATA[1], NC_000016.10:g.47115715_47115731AT[12]GTATATATATATATATATATATATATATA[1], NC_000016.10:g.47115715_47115731AT[12]GTATATATATATATATATATATATATATATA[1], NC_000016.10:g.47115715_47115731AT[12]GTATATATATATATATATATATATATATATATA[1], NC_000016.10:g.47115715_47115731AT[12]GTATATATATATATATATATATAT[2]A[1], NC_000016.10:g.47115715_47115731AT[12]GTATATATATATATATATATATGTGTATATATATATATATATATATA[1], NC_000016.10:g.47115715_47115731AT[12]GT[2]AT[8]A[1], NC_000016.10:g.47115715_47115731AT[12]GT[2]AT[10]A[1], NC_000016.10:g.47115715_47115731AT[11]GTATATATATATATATATATATA[1], NC_000016.10:g.47115715_47115731AT[11]GTATATATATATATATATATATATA[1], NC_000016.10:g.47115715_47115731ATATATATATATATATATATATGT[2]AT[10]A[1], NC_000016.10:g.47115715_47115731AT[11]GTATATATATATATATATATAT[2]A[1], NC_000016.10:g.47115715_47115731AT[11]GTATATATATATATATATATATGTGTATATATATATATATATATA[1], NC_000016.10:g.47115715_47115731ATATATATATATATATATATGT[2]AT[10]A[1], NC_000016.10:g.47115715_47115731AT[9]GTATATATATATATATATATATATA[1], NC_000016.10:g.47115715_47115731ATATATATATATATATATGTATAT[2]AT[9]A[1], NC_000016.10:g.47115715_47115731AT[9]GT[2]AT[10]A[1], NC_000016.9:g.47149627TA[5], NC_000016.9:g.47149627TA[6], NC_000016.9:g.47149627TA[7], NC_000016.9:g.47149627TA[9], NC_000016.9:g.47149626_47149642AT[9]ACATGTATATATATATACATATATATATATATATATA[1], NC_000016.9:g.47149627TA[10], NC_000016.9:g.47149626_47149642AT[10]ACATGTATATATATATACATATATATATATATATATA[1], NC_000016.9:g.47149627TA[11], NC_000016.9:g.47149627TA[12], NC_000016.9:g.47149627TA[13], NC_000016.9:g.47149627TA[15], NC_000016.9:g.47149627TA[18], NC_000016.9:g.47149627TA[19], NC_000016.9:g.47149626_47149642AT[14]GTATATATATATATATATA[1], NC_000016.9:g.47149626_47149642AT[14]GTATATATATATATATATATATATA[1], NC_000016.9:g.47149626_47149642AT[13]GTATATATATATATATATA[1], NC_000016.9:g.47149626_47149642AT[13]GTATATATATATATATATATATATA[1], NC_000016.9:g.47149626_47149642AT[13]GTATATATATATATATATATATATATA[1], NC_000016.9:g.47149626_47149642AT[13]GTATATATATATATATATATATATATATA[1], NC_000016.9:g.47149626_47149642AT[13]GTATATATATATATATATATATATATATATA[1], NC_000016.9:g.47149626_47149642AT[12]GTATAGATATATATATATATATATA[1], NC_000016.9:g.47149626_47149642AT[12]GTATATATATATATATATATATA[1], NC_000016.9:g.47149626_47149642AT[12]GTATATATATATATATATATATATA[1], NC_000016.9:g.47149626_47149642AT[12]GTATATATATATATATATATATATATA[1], NC_000016.9:g.47149626_47149642AT[12]GTATATATATATATATATATATATATATA[1], NC_000016.9:g.47149626_47149642AT[12]GTATATATATATATATATATATATATATATA[1], NC_000016.9:g.47149626_47149642AT[12]GTATATATATATATATATATATATATATATATA[1], NC_000016.9:g.47149626_47149642AT[12]GTATATATATATATATATATATAT[2]A[1], NC_000016.9:g.47149626_47149642AT[12]GTATATATATATATATATATATGTGTATATATATATATATATATATA[1], NC_000016.9:g.47149626_47149642AT[12]GT[2]AT[8]A[1], NC_000016.9:g.47149626_47149642AT[12]GT[2]AT[10]A[1], NC_000016.9:g.47149626_47149642AT[11]GTATATATATATATATATATATA[1], NC_000016.9:g.47149626_47149642AT[11]GTATATATATATATATATATATATA[1], NC_000016.9:g.47149626_47149642ATATATATATATATATATATATGT[2]AT[10]A[1], NC_000016.9:g.47149626_47149642AT[11]GTATATATATATATATATATAT[2]A[1], NC_000016.9:g.47149626_47149642AT[11]GTATATATATATATATATATATGTGTATATATATATATATATATA[1], NC_000016.9:g.47149626_47149642ATATATATATATATATATATGT[2]AT[10]A[1], NC_000016.9:g.47149626_47149642AT[9]GTATATATATATATATATATATATA[1], NC_000016.9:g.47149626_47149642ATATATATATATATATATGTATAT[2]AT[9]A[1], NC_000016.9:g.47149626_47149642AT[9]GT[2]AT[10]A[1], NG_047201.1:g.33296AT[5], NG_047201.1:g.33296AT[6], NG_047201.1:g.33296AT[7], NG_047201.1:g.33296AT[9], NG_047201.1:g.33295_33311TA[9]TGTATATATATATACATGTATATATATATATATATAT[1], NG_047201.1:g.33296AT[10], NG_047201.1:g.33295_33311TA[9]TGTATATATATATACATGTATATATATATATATATATAT[1], NG_047201.1:g.33296AT[11], NG_047201.1:g.33296AT[12], NG_047201.1:g.33296AT[13], NG_047201.1:g.33296AT[15], NG_047201.1:g.33296AT[18], NG_047201.1:g.33296AT[19], NG_047201.1:g.33295_33311TA[9]CATATATATATATATATATATATATATAT[1], NG_047201.1:g.33295_33311TA[12]CATATATATATATATATATATATATATAT[1], NG_047201.1:g.33295_33311TA[9]CATATATATATATATATATATATATAT[1], NG_047201.1:g.33295_33311TA[12]CATATATATATATATATATATATATAT[1], NG_047201.1:g.33295_33311TA[13]CATATATATATATATATATATATATAT[1], NG_047201.1:g.33295_33311TA[14]CATATATATATATATATATATATATAT[1], NG_047201.1:g.33295_33311TA[15]CATATATATATATATATATATATATAT[1], NG_047201.1:g.33295_33311TA[9]TCTATACATATATATATATATATATATATAT[1], NG_047201.1:g.33295_33311TA[11]CATATATATATATATATATATATAT[1], NG_047201.1:g.33295_33311TA[12]CATATATATATATATATATATATAT[1], NG_047201.1:g.33295_33311TA[13]CATATATATATATATATATATATAT[1], NG_047201.1:g.33295_33311TA[14]CATATATATATATATATATATATAT[1], NG_047201.1:g.33295_33311TA[15]CATATATATATATATATATATATAT[1], NG_047201.1:g.33295_33311TA[16]CATATATATATATATATATATATAT[1], NG_047201.1:g.33295_33311TA[12]CATATATATATATATATATATATA[2]T[1], NG_047201.1:g.33295_33311TA[11]CA[2]TA[10]CATATATATATATATATATATATAT[1], NG_047201.1:g.33295_33311TA[9]CA[2]TA[11]T[1], NG_047201.1:g.33295_33311TA[11]CA[2]TA[11]T[1], NG_047201.1:g.33295_33311TA[11]CATATATATATATATATATATAT[1], NG_047201.1:g.33295_33311TA[12]CATATATATATATATATATATAT[1], NG_047201.1:g.33295_33311TATATATATATATATATATATACA[2]TA[10]T[1], NG_047201.1:g.33295_33311TA[11]CATATATATATATATATATATA[2]T[1], NG_047201.1:g.33295_33311TA[10]CA[2]TA[10]CATATATATATATATATATATAT[1], NG_047201.1:g.33295_33311TA[11]CATATATATATATATATATATACATATATATATATATATATAT[1], NG_047201.1:g.33295_33311TA[12]CATATATATATATATATAT[1], NG_047201.1:g.33295_33311TA[12]CATATATATATATATATATATATACATATATATATATATATAT[1], NG_047201.1:g.33295_33311TA[11]CA[2]TA[8]T[1]

      3.

      rs1491197753 [Homo sapiens]
        Variant type:
        DEL
        Alleles:
        AT>- [Show Flanks]
        Chromosome:
        16:47115733 (GRCh38)
        16:47149644 (GRCh37)
        Canonical SPDI:
        NC_000016.10:47115732:AT:
        Gene:
        NETO2 (Varview)
        Functional Consequence:
        intron_variant
        Validated:
        by frequency,by alfa
        MAF:
        -=0./0 (ALFA)
        -=0.000008/1 (GnomAD)
        HGVS:

        4.

        rs1490966866 [Homo sapiens]
          Variant type:
          SNV
          Alleles:
          T>C [Show Flanks]
          Chromosome:
          16:47102013 (GRCh38)
          16:47135924 (GRCh37)
          Canonical SPDI:
          NC_000016.10:47102012:T:C
          Gene:
          NETO2 (Varview)
          Functional Consequence:
          intron_variant
          Validated:
          by frequency,by alfa,by cluster
          MAF:
          C=0./0 (ALFA)
          C=0.000019/5 (TOPMED)
          C=0.000021/3 (GnomAD)
          HGVS:

          5.

          rs1490891225 [Homo sapiens]
            Variant type:
            SNV
            Alleles:
            A>G [Show Flanks]
            Chromosome:
            16:47132478 (GRCh38)
            16:47166389 (GRCh37)
            Canonical SPDI:
            NC_000016.10:47132477:A:G
            Gene:
            NETO2 (Varview)
            Functional Consequence:
            intron_variant
            Validated:
            by frequency,by alfa
            MAF:
            G=0./0 (ALFA)
            G=0.000004/1 (TOPMED)
            HGVS:

            6.

            rs1490830912 [Homo sapiens]
              Variant type:
              SNV
              Alleles:
              T>A [Show Flanks]
              Chromosome:
              16:47123937 (GRCh38)
              16:47157848 (GRCh37)
              Canonical SPDI:
              NC_000016.10:47123936:T:A
              Gene:
              NETO2 (Varview)
              Functional Consequence:
              intron_variant
              Validated:
              by frequency,by alfa,by cluster
              MAF:
              A=0./0 (ALFA)
              A=0.000007/1 (GnomAD)
              A=0.000008/2 (TOPMED)
              HGVS:

              7.

              rs1490817195 [Homo sapiens]
                Variant type:
                SNV
                Alleles:
                T>C [Show Flanks]
                Chromosome:
                16:47125055 (GRCh38)
                16:47158966 (GRCh37)
                Canonical SPDI:
                NC_000016.10:47125054:T:C
                Gene:
                NETO2 (Varview)
                Functional Consequence:
                intron_variant
                Validated:
                by frequency,by alfa
                MAF:
                C=0./0 (ALFA)
                HGVS:

                8.

                rs1490710648 [Homo sapiens]
                  Variant type:
                  SNV
                  Alleles:
                  T>C [Show Flanks]
                  Chromosome:
                  16:47140235 (GRCh38)
                  16:47174146 (GRCh37)
                  Canonical SPDI:
                  NC_000016.10:47140234:T:C
                  Gene:
                  NETO2 (Varview)
                  Functional Consequence:
                  intron_variant,genic_upstream_transcript_variant
                  Validated:
                  by frequency,by alfa,by cluster
                  MAF:
                  C=0./0 (ALFA)
                  C=0.000007/1 (GnomAD)
                  C=0.000008/2 (TOPMED)
                  HGVS:

                  9.

                  rs1490634852 [Homo sapiens]
                    Variant type:
                    SNV:
                    Alleles:
                    A>G
                    Chromosome:
                    no mapping
                    Canonical SPDI:

                    10.

                    rs1490627927 [Homo sapiens]
                      Variant type:
                      SNV
                      Alleles:
                      G>A [Show Flanks]
                      Chromosome:
                      16:47097260 (GRCh38)
                      16:47131171 (GRCh37)
                      Canonical SPDI:
                      NC_000016.10:47097259:G:A
                      Gene:
                      NETO2 (Varview)
                      Functional Consequence:
                      intron_variant
                      Validated:
                      by frequency,by alfa
                      MAF:
                      A=0./0 (ALFA)
                      A=0.000007/1 (GnomAD)
                      HGVS:

                      11.

                      rs1490626510 [Homo sapiens]
                        Variant type:
                        SNV
                        Alleles:
                        T>C [Show Flanks]
                        Chromosome:
                        16:47110582 (GRCh38)
                        16:47144493 (GRCh37)
                        Canonical SPDI:
                        NC_000016.10:47110581:T:C
                        Gene:
                        NETO2 (Varview)
                        Functional Consequence:
                        intron_variant
                        Validated:
                        by frequency,by alfa,by cluster
                        MAF:
                        C=0./0 (ALFA)
                        C=0.000004/1 (TOPMED)
                        C=0.000007/1 (GnomAD)
                        HGVS:

                        12.

                        rs1490604069 [Homo sapiens]
                          Variant type:
                          SNV
                          Alleles:
                          C>G [Show Flanks]
                          Chromosome:
                          16:47124402 (GRCh38)
                          16:47158313 (GRCh37)
                          Canonical SPDI:
                          NC_000016.10:47124401:C:G
                          Gene:
                          NETO2 (Varview)
                          Functional Consequence:
                          intron_variant
                          Validated:
                          by frequency,by alfa
                          MAF:
                          G=0./0 (ALFA)
                          G=0.000004/1 (TOPMED)
                          HGVS:

                          13.

                          rs1490570873 [Homo sapiens]
                            Variant type:
                            SNV
                            Alleles:
                            G>C [Show Flanks]
                            Chromosome:
                            16:47086351 (GRCh38)
                            16:47120262 (GRCh37)
                            Canonical SPDI:
                            NC_000016.10:47086350:G:C
                            Gene:
                            NETO2 (Varview)
                            Functional Consequence:
                            intron_variant
                            Validated:
                            by frequency
                            MAF:
                            C=0.000004/1 (GnomAD_exomes)
                            HGVS:

                            14.

                            rs1490445114 [Homo sapiens]
                              Variant type:
                              SNV
                              Alleles:
                              A>G [Show Flanks]
                              Chromosome:
                              16:47133541 (GRCh38)
                              16:47167452 (GRCh37)
                              Canonical SPDI:
                              NC_000016.10:47133540:A:G
                              Gene:
                              NETO2 (Varview)
                              Functional Consequence:
                              intron_variant
                              Validated:
                              by frequency,by alfa
                              MAF:
                              G=0./0 (ALFA)
                              HGVS:

                              15.

                              rs1490419624 [Homo sapiens]
                                Variant type:
                                SNV
                                Alleles:
                                G>A,T [Show Flanks]
                                Chromosome:
                                16:47094023 (GRCh38)
                                16:47127934 (GRCh37)
                                Canonical SPDI:
                                NC_000016.10:47094022:G:A,NC_000016.10:47094022:G:T
                                Gene:
                                NETO2 (Varview)
                                Functional Consequence:
                                intron_variant
                                Validated:
                                by frequency,by alfa
                                MAF:
                                T=0./0 (ALFA)
                                A=0.000007/1 (GnomAD)
                                HGVS:

                                16.

                                rs1490328737 [Homo sapiens]
                                  Variant type:
                                  SNV
                                  Alleles:
                                  C>G,T [Show Flanks]
                                  Chromosome:
                                  16:47138735 (GRCh38)
                                  16:47172646 (GRCh37)
                                  Canonical SPDI:
                                  NC_000016.10:47138734:C:G,NC_000016.10:47138734:C:T
                                  Gene:
                                  NETO2 (Varview)
                                  Functional Consequence:
                                  intron_variant,genic_upstream_transcript_variant
                                  Validated:
                                  by frequency,by alfa,by cluster
                                  MAF:
                                  T=0./0 (ALFA)
                                  HGVS:

                                  17.

                                  rs1490308417 [Homo sapiens]
                                    Variant type:
                                    SNV
                                    Alleles:
                                    A>G [Show Flanks]
                                    Chromosome:
                                    16:47098775 (GRCh38)
                                    16:47132686 (GRCh37)
                                    Canonical SPDI:
                                    NC_000016.10:47098774:A:G
                                    Gene:
                                    NETO2 (Varview)
                                    Functional Consequence:
                                    intron_variant
                                    Validated:
                                    by frequency,by alfa,by cluster
                                    MAF:
                                    G=0./0 (ALFA)
                                    G=0.000007/1 (GnomAD)
                                    G=0.000008/2 (TOPMED)
                                    HGVS:

                                    18.

                                    rs1490301584 [Homo sapiens]
                                      Variant type:
                                      SNV
                                      Alleles:
                                      T>C [Show Flanks]
                                      Chromosome:
                                      16:47109715 (GRCh38)
                                      16:47143626 (GRCh37)
                                      Canonical SPDI:
                                      NC_000016.10:47109714:T:C
                                      Gene:
                                      NETO2 (Varview)
                                      Functional Consequence:
                                      intron_variant
                                      Validated:
                                      by frequency,by alfa,by cluster
                                      MAF:
                                      C=0.000071/1 (ALFA)
                                      C=0.000007/1 (GnomAD)
                                      C=0.000008/2 (TOPMED)
                                      HGVS:

                                      19.

                                      rs1490236047 [Homo sapiens]
                                        Variant type:
                                        SNV
                                        Alleles:
                                        A>T [Show Flanks]
                                        Chromosome:
                                        16:47122873 (GRCh38)
                                        16:47156784 (GRCh37)
                                        Canonical SPDI:
                                        NC_000016.10:47122872:A:T
                                        Gene:
                                        NETO2 (Varview), LOC124903806 (Varview)
                                        Functional Consequence:
                                        intron_variant,missense_variant,coding_sequence_variant,2KB_upstream_variant,upstream_transcript_variant
                                        Validated:
                                        by frequency,by alfa,by cluster
                                        MAF:
                                        T=0./0 (ALFA)
                                        T=0.000007/1 (GnomAD)
                                        HGVS:

                                        20.

                                        rs1490145300 [Homo sapiens]
                                          Variant type:
                                          SNV
                                          Alleles:
                                          C>T [Show Flanks]
                                          Chromosome:
                                          16:47139260 (GRCh38)
                                          16:47173171 (GRCh37)
                                          Canonical SPDI:
                                          NC_000016.10:47139259:C:T
                                          Gene:
                                          NETO2 (Varview)
                                          Functional Consequence:
                                          intron_variant,genic_upstream_transcript_variant
                                          HGVS:

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