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1.

rs1491522263 has merged into rs34215720 [Homo sapiens]
    Variant type:
    DELINS
    Alleles:
    TTTTTTTTTTTTTT>-,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
    Chromosome:
    10:86697226 (GRCh38)
    10:88456983 (GRCh37)
    Canonical SPDI:
    NC_000010.11:86697215:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000010.11:86697215:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000010.11:86697215:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000010.11:86697215:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000010.11:86697215:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000010.11:86697215:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000010.11:86697215:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000010.11:86697215:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000010.11:86697215:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000010.11:86697215:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000010.11:86697215:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000010.11:86697215:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:86697215:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:86697215:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:86697215:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:86697215:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:86697215:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:86697215:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:86697215:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:86697215:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:86697215:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:86697215:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:86697215:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:86697215:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:86697215:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:86697215:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:86697215:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:86697215:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:86697215:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:86697215:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:86697215:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
    Gene:
    LDB3 (Varview)
    Functional Consequence:
    intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    TTTTTTTTTT=0./0 (ALFA)
    HGVS:
    NC_000010.11:g.86697226_86697239del, NC_000010.11:g.86697228_86697239del, NC_000010.11:g.86697229_86697239del, NC_000010.11:g.86697230_86697239del, NC_000010.11:g.86697231_86697239del, NC_000010.11:g.86697232_86697239del, NC_000010.11:g.86697233_86697239del, NC_000010.11:g.86697234_86697239del, NC_000010.11:g.86697235_86697239del, NC_000010.11:g.86697236_86697239del, NC_000010.11:g.86697237_86697239del, NC_000010.11:g.86697238_86697239del, NC_000010.11:g.86697239del, NC_000010.11:g.86697239dup, NC_000010.11:g.86697238_86697239dup, NC_000010.11:g.86697237_86697239dup, NC_000010.11:g.86697236_86697239dup, NC_000010.11:g.86697235_86697239dup, NC_000010.11:g.86697234_86697239dup, NC_000010.11:g.86697233_86697239dup, NC_000010.11:g.86697232_86697239dup, NC_000010.11:g.86697231_86697239dup, NC_000010.11:g.86697230_86697239dup, NC_000010.11:g.86697229_86697239dup, NC_000010.11:g.86697228_86697239dup, NC_000010.11:g.86697227_86697239dup, NC_000010.11:g.86697226_86697239dup, NC_000010.11:g.86697225_86697239dup, NC_000010.11:g.86697224_86697239dup, NC_000010.11:g.86697239_86697240insTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.11:g.86697239_86697240insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.10:g.88456983_88456996del, NC_000010.10:g.88456985_88456996del, NC_000010.10:g.88456986_88456996del, NC_000010.10:g.88456987_88456996del, NC_000010.10:g.88456988_88456996del, NC_000010.10:g.88456989_88456996del, NC_000010.10:g.88456990_88456996del, NC_000010.10:g.88456991_88456996del, NC_000010.10:g.88456992_88456996del, NC_000010.10:g.88456993_88456996del, NC_000010.10:g.88456994_88456996del, NC_000010.10:g.88456995_88456996del, NC_000010.10:g.88456996del, NC_000010.10:g.88456996dup, NC_000010.10:g.88456995_88456996dup, NC_000010.10:g.88456994_88456996dup, NC_000010.10:g.88456993_88456996dup, NC_000010.10:g.88456992_88456996dup, NC_000010.10:g.88456991_88456996dup, NC_000010.10:g.88456990_88456996dup, NC_000010.10:g.88456989_88456996dup, NC_000010.10:g.88456988_88456996dup, NC_000010.10:g.88456987_88456996dup, NC_000010.10:g.88456986_88456996dup, NC_000010.10:g.88456985_88456996dup, NC_000010.10:g.88456984_88456996dup, NC_000010.10:g.88456983_88456996dup, NC_000010.10:g.88456982_88456996dup, NC_000010.10:g.88456981_88456996dup, NC_000010.10:g.88456996_88456997insTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.10:g.88456996_88456997insTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_008876.1:g.33663_33676del, NG_008876.1:g.33665_33676del, NG_008876.1:g.33666_33676del, NG_008876.1:g.33667_33676del, NG_008876.1:g.33668_33676del, NG_008876.1:g.33669_33676del, NG_008876.1:g.33670_33676del, NG_008876.1:g.33671_33676del, NG_008876.1:g.33672_33676del, NG_008876.1:g.33673_33676del, NG_008876.1:g.33674_33676del, NG_008876.1:g.33675_33676del, NG_008876.1:g.33676del, NG_008876.1:g.33676dup, NG_008876.1:g.33675_33676dup, NG_008876.1:g.33674_33676dup, NG_008876.1:g.33673_33676dup, NG_008876.1:g.33672_33676dup, NG_008876.1:g.33671_33676dup, NG_008876.1:g.33670_33676dup, NG_008876.1:g.33669_33676dup, NG_008876.1:g.33668_33676dup, NG_008876.1:g.33667_33676dup, NG_008876.1:g.33666_33676dup, NG_008876.1:g.33665_33676dup, NG_008876.1:g.33664_33676dup, NG_008876.1:g.33663_33676dup, NG_008876.1:g.33662_33676dup, NG_008876.1:g.33661_33676dup, NG_008876.1:g.33676_33677insTTTTTTTTTTTTTTTTTTTTTTTTT, NG_008876.1:g.33676_33677insTTTTTTTTTTTTTTTTTTTTTTTTTT

    2.

    rs1491464254 has merged into rs11314847 [Homo sapiens]
      Variant type:
      DELINS
      Alleles:
      AAAA>-,A,AA,AAA,AAAAA,AAAAAA,AAAAAAAAAAAAAAA [Show Flanks]
      Chromosome:
      10:86735006 (GRCh38)
      10:88494763 (GRCh37)
      Canonical SPDI:
      NC_000010.11:86734994:AAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000010.11:86734994:AAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000010.11:86734994:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000010.11:86734994:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000010.11:86734994:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000010.11:86734994:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000010.11:86734994:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA
      Gene:
      LDB3 (Varview)
      Functional Consequence:
      genic_downstream_transcript_variant,3_prime_UTR_variant
      Validated:
      by frequency,by alfa,by cluster
      MAF:
      AAAAAAAAAAAAA=0./0 (ALFA)
      A=0.1416/709 (1000Genomes)
      HGVS:
      NC_000010.11:g.86735006_86735009del, NC_000010.11:g.86735007_86735009del, NC_000010.11:g.86735008_86735009del, NC_000010.11:g.86735009del, NC_000010.11:g.86735009dup, NC_000010.11:g.86735008_86735009dup, NC_000010.11:g.86734999_86735009dup, NC_000010.10:g.88494763_88494766del, NC_000010.10:g.88494764_88494766del, NC_000010.10:g.88494765_88494766del, NC_000010.10:g.88494766del, NC_000010.10:g.88494766dup, NC_000010.10:g.88494765_88494766dup, NC_000010.10:g.88494756_88494766dup, NG_008876.1:g.71443_71446del, NG_008876.1:g.71444_71446del, NG_008876.1:g.71445_71446del, NG_008876.1:g.71446del, NG_008876.1:g.71446dup, NG_008876.1:g.71445_71446dup, NG_008876.1:g.71436_71446dup, NM_007078.3:c.*2030_*2033del, NM_007078.3:c.*2031_*2033del, NM_007078.3:c.*2032_*2033del, NM_007078.3:c.*2033del, NM_007078.3:c.*2033dup, NM_007078.3:c.*2032_*2033dup, NM_007078.3:c.*2023_*2033dup, NM_007078.2:c.*2030_*2033del, NM_007078.2:c.*2031_*2033del, NM_007078.2:c.*2032_*2033del, NM_007078.2:c.*2033del, NM_007078.2:c.*2033dup, NM_007078.2:c.*2032_*2033dup, NM_007078.2:c.*2023_*2033dup, NM_001171610.2:c.*2030_*2033del, NM_001171610.2:c.*2031_*2033del, NM_001171610.2:c.*2032_*2033del, NM_001171610.2:c.*2033del, NM_001171610.2:c.*2033dup, NM_001171610.2:c.*2032_*2033dup, NM_001171610.2:c.*2023_*2033dup, NM_001171610.1:c.*2030_*2033del, NM_001171610.1:c.*2031_*2033del, NM_001171610.1:c.*2032_*2033del, NM_001171610.1:c.*2033del, NM_001171610.1:c.*2033dup, NM_001171610.1:c.*2032_*2033dup, NM_001171610.1:c.*2023_*2033dup, NM_001080114.2:c.*2030_*2033del, NM_001080114.2:c.*2031_*2033del, NM_001080114.2:c.*2032_*2033del, NM_001080114.2:c.*2033del, NM_001080114.2:c.*2033dup, NM_001080114.2:c.*2032_*2033dup, NM_001080114.2:c.*2023_*2033dup, NM_001080114.1:c.*2030_*2033del, NM_001080114.1:c.*2031_*2033del, NM_001080114.1:c.*2032_*2033del, NM_001080114.1:c.*2033del, NM_001080114.1:c.*2033dup, NM_001080114.1:c.*2032_*2033dup, NM_001080114.1:c.*2023_*2033dup, NM_001368066.1:c.*2030_*2033del, NM_001368066.1:c.*2031_*2033del, NM_001368066.1:c.*2032_*2033del, NM_001368066.1:c.*2033del, NM_001368066.1:c.*2033dup, NM_001368066.1:c.*2032_*2033dup, NM_001368066.1:c.*2023_*2033dup, NM_001368064.1:c.*2030_*2033del, NM_001368064.1:c.*2031_*2033del, NM_001368064.1:c.*2032_*2033del, NM_001368064.1:c.*2033del, NM_001368064.1:c.*2033dup, NM_001368064.1:c.*2032_*2033dup, NM_001368064.1:c.*2023_*2033dup, NM_001368065.1:c.*2030_*2033del, NM_001368065.1:c.*2031_*2033del, NM_001368065.1:c.*2032_*2033del, NM_001368065.1:c.*2033del, NM_001368065.1:c.*2033dup, NM_001368065.1:c.*2032_*2033dup, NM_001368065.1:c.*2023_*2033dup

      3.

      rs1491446584 [Homo sapiens]
        Variant type:
        DEL
        Alleles:
        GA>- [Show Flanks]
        Chromosome:
        10:86734994 (GRCh38)
        10:88494751 (GRCh37)
        Canonical SPDI:
        NC_000010.11:86734993:GA:
        Gene:
        LDB3 (Varview)
        Functional Consequence:
        3_prime_UTR_variant,genic_downstream_transcript_variant
        Validated:
        by frequency,by alfa
        MAF:
        -=0./0 (ALFA)
        HGVS:

        4.

        rs1491338329 [Homo sapiens]
          Variant type:
          DEL
          Alleles:
          AT>- [Show Flanks]
          Chromosome:
          10:86664016 (GRCh38)
          10:88423773 (GRCh37)
          Canonical SPDI:
          NC_000010.11:86664015:AT:
          Gene:
          OPN4 (Varview), LOC105378409 (Varview)
          Functional Consequence:
          3_prime_UTR_variant,intron_variant
          Validated:
          by frequency,by alfa,by cluster
          MAF:
          -=0.042052/754 (ALFA)
          -=0.000035/1 (TOMMO)
          -=0.02/12 (NorthernSweden)
          -=0.020612/103 (1000Genomes)
          -=0.034546/9144 (TOPMED)
          -=0.034714/1613 (GnomAD_exomes)
          -=0.035058/4892 (GnomAD)
          -=0.037763/79 (ExAC)
          -=0.041802/155 (TWINSUK)
          -=0.042084/42 (GoNL)
          -=0.045148/174 (ALSPAC)
          HGVS:

          5.

          rs1491272849 [Homo sapiens]
            Variant type:
            INS
            Alleles:
            ->A,AA,AAA [Show Flanks]
            Chromosome:
            10:86686805 (GRCh38)
            10:88446563 (GRCh37)
            Canonical SPDI:
            NC_000010.11:86686805::A,NC_000010.11:86686805::AA,NC_000010.11:86686805::AAA
            Gene:
            LDB3 (Varview)
            Functional Consequence:
            intron_variant
            Validated:
            by frequency,by alfa
            MAF:
            AA=0./0 (ALFA)
            AA=0.00103/29 (TOMMO)
            HGVS:

            6.

            rs1491198667 [Homo sapiens]
              Variant type:
              SNV:
              Alleles:
              TC>-
              Chromosome:
              no mapping
              Canonical SPDI:

              7.

              rs1491164939 [Homo sapiens]
                Variant type:
                DELINS
                Alleles:
                AA>-,A [Show Flanks]
                Chromosome:
                10:86716231 (GRCh38)
                10:88475988 (GRCh37)
                Canonical SPDI:
                NC_000010.11:86716229:AAA:A,NC_000010.11:86716229:AAA:AA
                Gene:
                LDB3 (Varview)
                Functional Consequence:
                genic_downstream_transcript_variant,intron_variant
                Validated:
                by frequency,by alfa,by cluster
                MAF:
                A=0./0 (ALFA)
                -=0.000004/1 (TOPMED)
                -=0.000035/1 (TOMMO)
                HGVS:

                8.

                rs1491086170 [Homo sapiens]
                  Variant type:
                  DEL
                  Alleles:
                  TG>- [Show Flanks]
                  Chromosome:
                  10:86697239 (GRCh38)
                  10:88456996 (GRCh37)
                  Canonical SPDI:
                  NC_000010.11:86697238:TG:
                  Gene:
                  LDB3 (Varview)
                  Functional Consequence:
                  intron_variant
                  Validated:
                  by frequency,by alfa
                  MAF:
                  -=0.000506/6 (ALFA)
                  -=0.000039/5 (GnomAD)
                  HGVS:

                  9.

                  rs1491059044 has merged into rs200011805 [Homo sapiens]
                    Variant type:
                    DELINS
                    Alleles:
                    AA>-,A,AAA,AAAA [Show Flanks]
                    Chromosome:
                    10:86724610 (GRCh38)
                    10:88484367 (GRCh37)
                    Canonical SPDI:
                    NC_000010.11:86724602:AAAAAAAAA:AAAAAAA,NC_000010.11:86724602:AAAAAAAAA:AAAAAAAA,NC_000010.11:86724602:AAAAAAAAA:AAAAAAAAAA,NC_000010.11:86724602:AAAAAAAAA:AAAAAAAAAAA
                    Gene:
                    LDB3 (Varview)
                    Functional Consequence:
                    intron_variant,genic_downstream_transcript_variant
                    Validated:
                    by frequency,by alfa,by cluster
                    MAF:
                    AAAAAAAA=0./0 (ALFA)
                    -=0.000083/22 (TOPMED)
                    A=0.000106/3 (TOMMO)
                    -=0.001421/7 (1000Genomes)
                    HGVS:

                    10.

                    rs1491021571 [Homo sapiens]
                      Variant type:
                      DELINS
                      Alleles:
                      AT>- [Show Flanks]
                      Chromosome:
                      10:86727844 (GRCh38)
                      10:88487601 (GRCh37)
                      Canonical SPDI:
                      NC_000010.11:86727842:TAT:T
                      Gene:
                      LDB3 (Varview)
                      Functional Consequence:
                      genic_downstream_transcript_variant,intron_variant
                      Validated:
                      by frequency,by alfa,by cluster
                      MAF:
                      T=0.01391/165 (ALFA)
                      -=0.00058/9 (TOMMO)
                      -=0.02145/1916 (GnomAD)
                      HGVS:

                      11.

                      rs1491003347 [Homo sapiens]
                        Variant type:
                        SNV
                        Alleles:
                        C>G [Show Flanks]
                        Chromosome:
                        10:86711718 (GRCh38)
                        10:88471475 (GRCh37)
                        Canonical SPDI:
                        NC_000010.11:86711717:C:G
                        Gene:
                        LDB3 (Varview)
                        Functional Consequence:
                        genic_downstream_transcript_variant,intron_variant
                        Validated:
                        by frequency,by alfa
                        MAF:
                        G=0./0 (ALFA)
                        HGVS:

                        12.

                        rs1490980960 [Homo sapiens]
                          Variant type:
                          SNV
                          Alleles:
                          A>T [Show Flanks]
                          Chromosome:
                          10:86687048 (GRCh38)
                          10:88446805 (GRCh37)
                          Canonical SPDI:
                          NC_000010.11:86687047:A:T
                          Gene:
                          LDB3 (Varview)
                          Functional Consequence:
                          intron_variant
                          Validated:
                          by frequency
                          MAF:
                          T=0.000004/1 (GnomAD_exomes)
                          HGVS:

                          13.

                          rs1490967606 [Homo sapiens]
                            Variant type:
                            SNV
                            Alleles:
                            A>G,T [Show Flanks]
                            Chromosome:
                            10:86715609 (GRCh38)
                            10:88475366 (GRCh37)
                            Canonical SPDI:
                            NC_000010.11:86715608:A:G,NC_000010.11:86715608:A:T
                            Gene:
                            LDB3 (Varview)
                            Functional Consequence:
                            genic_downstream_transcript_variant,intron_variant
                            Validated:
                            by frequency,by alfa,by cluster
                            MAF:
                            T=0.00011/2 (ALFA)
                            T=0.00045/2 (Estonian)
                            HGVS:

                            14.

                            rs1490932449 [Homo sapiens]
                              Variant type:
                              SNV
                              Alleles:
                              G>A [Show Flanks]
                              Chromosome:
                              10:86712468 (GRCh38)
                              10:88472225 (GRCh37)
                              Canonical SPDI:
                              NC_000010.11:86712467:G:A
                              Gene:
                              LDB3 (Varview)
                              Functional Consequence:
                              genic_downstream_transcript_variant,intron_variant
                              Validated:
                              by frequency,by alfa,by cluster
                              MAF:
                              A=0.000071/1 (ALFA)
                              A=0.000004/1 (TOPMED)
                              A=0.000007/1 (GnomAD)
                              HGVS:

                              15.

                              rs1490917572 [Homo sapiens]
                                Variant type:
                                SNV
                                Alleles:
                                A>G [Show Flanks]
                                Chromosome:
                                10:86682319 (GRCh38)
                                10:88442076 (GRCh37)
                                Canonical SPDI:
                                NC_000010.11:86682318:A:G
                                Gene:
                                LDB3 (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:

                                16.

                                rs1490888605 [Homo sapiens]
                                  Variant type:
                                  SNV
                                  Alleles:
                                  C>G [Show Flanks]
                                  Chromosome:
                                  10:86711559 (GRCh38)
                                  10:88471316 (GRCh37)
                                  Canonical SPDI:
                                  NC_000010.11:86711558:C:G
                                  Gene:
                                  LDB3 (Varview)
                                  Functional Consequence:
                                  genic_downstream_transcript_variant,intron_variant
                                  Validated:
                                  by frequency,by alfa,by cluster
                                  MAF:
                                  G=0.000071/1 (ALFA)
                                  G=0.000014/2 (GnomAD)
                                  G=0.00003/8 (TOPMED)
                                  HGVS:

                                  17.

                                  rs1490863262 [Homo sapiens]
                                    Variant type:
                                    SNV
                                    Alleles:
                                    G>A,C [Show Flanks]
                                    Chromosome:
                                    10:86697104 (GRCh38)
                                    10:88456861 (GRCh37)
                                    Canonical SPDI:
                                    NC_000010.11:86697103:G:A,NC_000010.11:86697103:G:C
                                    Gene:
                                    LDB3 (Varview)
                                    Functional Consequence:
                                    intron_variant
                                    Validated:
                                    by frequency,by alfa,by cluster
                                    MAF:
                                    C=0./0 (ALFA)
                                    HGVS:

                                    18.

                                    rs1490857136 [Homo sapiens]
                                      Variant type:
                                      SNV
                                      Alleles:
                                      C>T [Show Flanks]
                                      Chromosome:
                                      10:86713371 (GRCh38)
                                      10:88473128 (GRCh37)
                                      Canonical SPDI:
                                      NC_000010.11:86713370:C:T
                                      Gene:
                                      LDB3 (Varview)
                                      Functional Consequence:
                                      genic_downstream_transcript_variant,intron_variant
                                      Validated:
                                      by frequency,by alfa,by cluster
                                      MAF:
                                      T=0./0 (ALFA)
                                      T=0.000035/1 (TOMMO)
                                      T=0.000036/5 (GnomAD)
                                      T=0.000053/14 (TOPMED)
                                      T=0.000546/1 (Korea1K)
                                      C=0.5/1 (SGDP_PRJ)
                                      HGVS:

                                      19.

                                      rs1490853980 [Homo sapiens]
                                        Variant type:
                                        DEL
                                        Alleles:
                                        CT>- [Show Flanks]
                                        Chromosome:
                                        10:86696156 (GRCh38)
                                        10:88455913 (GRCh37)
                                        Canonical SPDI:
                                        NC_000010.11:86696155:CT:
                                        Gene:
                                        LDB3 (Varview)
                                        Functional Consequence:
                                        intron_variant
                                        Validated:
                                        by frequency,by alfa,by cluster
                                        MAF:
                                        -=0./0 (ALFA)
                                        -=0.000007/1 (GnomAD)
                                        -=0.000015/4 (TOPMED)
                                        HGVS:

                                        20.

                                        rs1490820772 [Homo sapiens]
                                          Variant type:
                                          SNV
                                          Alleles:
                                          T>C [Show Flanks]
                                          Chromosome:
                                          10:86696501 (GRCh38)
                                          10:88456258 (GRCh37)
                                          Canonical SPDI:
                                          NC_000010.11:86696500:T:C
                                          Gene:
                                          LDB3 (Varview)
                                          Functional Consequence:
                                          intron_variant
                                          Validated:
                                          by frequency,by alfa,by cluster
                                          MAF:
                                          C=0./0 (ALFA)
                                          C=0.000004/1 (TOPMED)
                                          C=0.000014/2 (GnomAD)
                                          HGVS:

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