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Items: 1 to 20 of 8498

1.

rs1491586517 has merged into rs5859643 [Homo sapiens]
    Variant type:
    DELINS
    Alleles:
    AAA>-,A,AA,AAAA,AAAAA,AAAAAA,AAAAAAAAA,AAAAAAAAAAAAAAA [Show Flanks]
    Chromosome:
    4:78652172 (GRCh38)
    4:79573326 (GRCh37)
    Canonical SPDI:
    NC_000004.12:78652159:AAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000004.12:78652159:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000004.12:78652159:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000004.12:78652159:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000004.12:78652159:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000004.12:78652159:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000004.12:78652159:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000004.12:78652159:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA
    Gene:
    LINC01094 (Varview)
    Functional Consequence:
    intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    AAAAAAAAAAAAAAAA=0./0 (ALFA)
    A=0./0 (ALSPAC)
    A=0./0 (TWINSUK)
    A=0.1032/517 (1000Genomes)
    HGVS:

    2.

    rs1491576007 [Homo sapiens]
      Variant type:
      DELINS
      Alleles:
      TT>- [Show Flanks]
      Chromosome:
      4:78648330 (GRCh38)
      4:79569484 (GRCh37)
      Canonical SPDI:
      NC_000004.12:78648328:TTT:T
      Gene:
      LINC01094 (Varview)
      Functional Consequence:
      intron_variant
      Validated:
      by frequency,by alfa,by cluster
      MAF:
      T=0.00043/7 (ALFA)
      -=0.00164/3 (Korea1K)
      -=0.00182/29 (TOMMO)
      HGVS:

      3.

      rs1491498904 [Homo sapiens]
        Variant type:
        INS
        Alleles:
        ->C [Show Flanks]
        Chromosome:
        4:78661969 (GRCh38)
        4:79583124 (GRCh37)
        Canonical SPDI:
        NC_000004.12:78661969::C
        Gene:
        LINC01094 (Varview)
        Functional Consequence:
        intron_variant
        Validated:
        by frequency,by alfa,by cluster
        MAF:
        C=0./0 (ALFA)
        C=0.000004/1 (TOPMED)
        C=0.000044/1 (GnomAD)
        HGVS:

        4.

        rs1491366193 [Homo sapiens]
          Variant type:
          SNV:
          Alleles:
          ->T
          Chromosome:
          no mapping
          Canonical SPDI:

          5.

          rs1491340139 has merged into rs34139607 [Homo sapiens]
            Variant type:
            DELINS
            Alleles:
            TTTTTTTT>-,TT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
            Chromosome:
            4:78661978 (GRCh38)
            4:79583132 (GRCh37)
            Canonical SPDI:
            NC_000004.12:78661968:TTTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000004.12:78661968:TTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000004.12:78661968:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000004.12:78661968:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000004.12:78661968:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000004.12:78661968:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000004.12:78661968:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000004.12:78661968:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000004.12:78661968:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000004.12:78661968:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:78661968:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:78661968:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:78661968:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:78661968:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:78661968:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:78661968:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:78661968:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:78661968:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:78661968:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:78661968:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:78661968:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:78661968:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:78661968:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:78661968:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:78661968:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:78661968:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:78661968:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:78661968:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:78661968:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:78661968:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
            Gene:
            LINC01094 (Varview)
            Functional Consequence:
            intron_variant
            Validated:
            by frequency,by alfa,by cluster
            MAF:
            TTTTTTTTTTT=0./0 (ALFA)
            -=0.000004/1 (TOPMED)
            -=0.205072/1027 (1000Genomes)
            HGVS:
            NC_000004.12:g.78661978_78661985del, NC_000004.12:g.78661980_78661985del, NC_000004.12:g.78661983_78661985del, NC_000004.12:g.78661984_78661985del, NC_000004.12:g.78661985del, NC_000004.12:g.78661985dup, NC_000004.12:g.78661984_78661985dup, NC_000004.12:g.78661983_78661985dup, NC_000004.12:g.78661982_78661985dup, NC_000004.12:g.78661981_78661985dup, NC_000004.12:g.78661980_78661985dup, NC_000004.12:g.78661978_78661985dup, NC_000004.12:g.78661977_78661985dup, NC_000004.12:g.78661976_78661985dup, NC_000004.12:g.78661975_78661985dup, NC_000004.12:g.78661974_78661985dup, NC_000004.12:g.78661972_78661985dup, NC_000004.12:g.78661971_78661985dup, NC_000004.12:g.78661970_78661985dup, NC_000004.12:g.78661969_78661985dup, NC_000004.12:g.78661985_78661986insTTTTTTTTTTTTTTTTTT, NC_000004.12:g.78661985_78661986insTTTTTTTTTTTTTTTTTTT, NC_000004.12:g.78661985_78661986insTTTTTTTTTTTTTTTTTTTT, NC_000004.12:g.78661985_78661986insTTTTTTTTTTTTTTTTTTTTTT, NC_000004.12:g.78661985_78661986insTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.12:g.78661985_78661986insTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.12:g.78661985_78661986insTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.12:g.78661985_78661986insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.12:g.78661985_78661986insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.12:g.78661985_78661986insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.79583132_79583139del, NC_000004.11:g.79583134_79583139del, NC_000004.11:g.79583137_79583139del, NC_000004.11:g.79583138_79583139del, NC_000004.11:g.79583139del, NC_000004.11:g.79583139dup, NC_000004.11:g.79583138_79583139dup, NC_000004.11:g.79583137_79583139dup, NC_000004.11:g.79583136_79583139dup, NC_000004.11:g.79583135_79583139dup, NC_000004.11:g.79583134_79583139dup, NC_000004.11:g.79583132_79583139dup, NC_000004.11:g.79583131_79583139dup, NC_000004.11:g.79583130_79583139dup, NC_000004.11:g.79583129_79583139dup, NC_000004.11:g.79583128_79583139dup, NC_000004.11:g.79583126_79583139dup, NC_000004.11:g.79583125_79583139dup, NC_000004.11:g.79583124_79583139dup, NC_000004.11:g.79583123_79583139dup, NC_000004.11:g.79583139_79583140insTTTTTTTTTTTTTTTTTT, NC_000004.11:g.79583139_79583140insTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.79583139_79583140insTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.79583139_79583140insTTTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.79583139_79583140insTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.79583139_79583140insTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.79583139_79583140insTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.79583139_79583140insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.79583139_79583140insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.79583139_79583140insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

            6.

            rs1491319946 [Homo sapiens]
              Variant type:
              DELINS
              Alleles:
              CC>-,CCCC [Show Flanks]
              Chromosome:
              4:78648315 (GRCh38)
              4:79569469 (GRCh37)
              Canonical SPDI:
              NC_000004.12:78648313:CCC:C,NC_000004.12:78648313:CCC:CCCCC
              Gene:
              LINC01094 (Varview)
              Functional Consequence:
              intron_variant
              Validated:
              by frequency,by alfa,by cluster
              MAF:
              C=0./0 (ALFA)
              -=0.00008/8 (GnomAD)
              HGVS:

              7.

              rs1491253193 [Homo sapiens]
                Variant type:
                DEL
                Alleles:
                CA>- [Show Flanks]
                Chromosome:
                4:78682699 (GRCh38)
                4:79603853 (GRCh37)
                Canonical SPDI:
                NC_000004.12:78682698:CA:
                Gene:
                LINC01094 (Varview)
                Functional Consequence:
                non_coding_transcript_variant
                Validated:
                by frequency,by alfa
                MAF:
                -=0.00194/23 (ALFA)
                HGVS:

                8.

                rs1491231642 [Homo sapiens]
                  Variant type:
                  DEL
                  Alleles:
                  CA>- [Show Flanks]
                  Chromosome:
                  4:78652159 (GRCh38)
                  4:79573313 (GRCh37)
                  Canonical SPDI:
                  NC_000004.12:78652158:CA:
                  Gene:
                  LINC01094 (Varview)
                  Functional Consequence:
                  intron_variant
                  Validated:
                  by frequency,by alfa
                  MAF:
                  -=0.00008/1 (ALFA)
                  HGVS:

                  9.

                  rs1491221355 has merged into rs33987465 [Homo sapiens]
                    Variant type:
                    DELINS
                    Alleles:
                    AAAAAAAAAAAAAAAA>-,A,AA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
                    Chromosome:
                    4:78682710 (GRCh38)
                    4:79603864 (GRCh37)
                    Canonical SPDI:
                    NC_000004.12:78682699:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000004.12:78682699:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000004.12:78682699:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000004.12:78682699:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000004.12:78682699:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000004.12:78682699:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000004.12:78682699:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000004.12:78682699:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000004.12:78682699:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000004.12:78682699:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:78682699:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:78682699:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:78682699:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:78682699:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:78682699:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:78682699:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:78682699:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:78682699:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:78682699:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:78682699:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
                    Gene:
                    LINC01094 (Varview)
                    Functional Consequence:
                    non_coding_transcript_variant
                    Validated:
                    by frequency,by alfa,by cluster
                    MAF:
                    AAAAAAAAAA=0./0 (ALFA)
                    AAA=0.4874/2441 (1000Genomes)
                    HGVS:
                    NC_000004.12:g.78682710_78682725del, NC_000004.12:g.78682711_78682725del, NC_000004.12:g.78682712_78682725del, NC_000004.12:g.78682714_78682725del, NC_000004.12:g.78682715_78682725del, NC_000004.12:g.78682716_78682725del, NC_000004.12:g.78682717_78682725del, NC_000004.12:g.78682718_78682725del, NC_000004.12:g.78682721_78682725del, NC_000004.12:g.78682722_78682725del, NC_000004.12:g.78682723_78682725del, NC_000004.12:g.78682724_78682725del, NC_000004.12:g.78682725del, NC_000004.12:g.78682725dup, NC_000004.12:g.78682724_78682725dup, NC_000004.12:g.78682723_78682725dup, NC_000004.12:g.78682722_78682725dup, NC_000004.12:g.78682721_78682725dup, NC_000004.12:g.78682720_78682725dup, NC_000004.12:g.78682725_78682726insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000004.11:g.79603864_79603879del, NC_000004.11:g.79603865_79603879del, NC_000004.11:g.79603866_79603879del, NC_000004.11:g.79603868_79603879del, NC_000004.11:g.79603869_79603879del, NC_000004.11:g.79603870_79603879del, NC_000004.11:g.79603871_79603879del, NC_000004.11:g.79603872_79603879del, NC_000004.11:g.79603875_79603879del, NC_000004.11:g.79603876_79603879del, NC_000004.11:g.79603877_79603879del, NC_000004.11:g.79603878_79603879del, NC_000004.11:g.79603879del, NC_000004.11:g.79603879dup, NC_000004.11:g.79603878_79603879dup, NC_000004.11:g.79603877_79603879dup, NC_000004.11:g.79603876_79603879dup, NC_000004.11:g.79603875_79603879dup, NC_000004.11:g.79603874_79603879dup, NC_000004.11:g.79603879_79603880insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NR_038303.1:n.2495_2510del, NR_038303.1:n.2496_2510del, NR_038303.1:n.2497_2510del, NR_038303.1:n.2499_2510del, NR_038303.1:n.2500_2510del, NR_038303.1:n.2501_2510del, NR_038303.1:n.2502_2510del, NR_038303.1:n.2503_2510del, NR_038303.1:n.2506_2510del, NR_038303.1:n.2507_2510del, NR_038303.1:n.2508_2510del, NR_038303.1:n.2509_2510del, NR_038303.1:n.2510del, NR_038303.1:n.2510dup, NR_038303.1:n.2509_2510dup, NR_038303.1:n.2508_2510dup, NR_038303.1:n.2507_2510dup, NR_038303.1:n.2506_2510dup, NR_038303.1:n.2505_2510dup, NR_038303.1:n.2510_2511insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NR_038304.1:n.2423_2438del, NR_038304.1:n.2424_2438del, NR_038304.1:n.2425_2438del, NR_038304.1:n.2427_2438del, NR_038304.1:n.2428_2438del, NR_038304.1:n.2429_2438del, NR_038304.1:n.2430_2438del, NR_038304.1:n.2431_2438del, NR_038304.1:n.2434_2438del, NR_038304.1:n.2435_2438del, NR_038304.1:n.2436_2438del, NR_038304.1:n.2437_2438del, NR_038304.1:n.2438del, NR_038304.1:n.2438dup, NR_038304.1:n.2437_2438dup, NR_038304.1:n.2436_2438dup, NR_038304.1:n.2435_2438dup, NR_038304.1:n.2434_2438dup, NR_038304.1:n.2433_2438dup, NR_038304.1:n.2438_2439insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NR_038305.1:n.2401_2416del, NR_038305.1:n.2402_2416del, NR_038305.1:n.2403_2416del, NR_038305.1:n.2405_2416del, NR_038305.1:n.2406_2416del, NR_038305.1:n.2407_2416del, NR_038305.1:n.2408_2416del, NR_038305.1:n.2409_2416del, NR_038305.1:n.2412_2416del, NR_038305.1:n.2413_2416del, NR_038305.1:n.2414_2416del, NR_038305.1:n.2415_2416del, NR_038305.1:n.2416del, NR_038305.1:n.2416dup, NR_038305.1:n.2415_2416dup, NR_038305.1:n.2414_2416dup, NR_038305.1:n.2413_2416dup, NR_038305.1:n.2412_2416dup, NR_038305.1:n.2411_2416dup, NR_038305.1:n.2416_2417insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NR_038306.1:n.2329_2344del, NR_038306.1:n.2330_2344del, NR_038306.1:n.2331_2344del, NR_038306.1:n.2333_2344del, NR_038306.1:n.2334_2344del, NR_038306.1:n.2335_2344del, NR_038306.1:n.2336_2344del, NR_038306.1:n.2337_2344del, NR_038306.1:n.2340_2344del, NR_038306.1:n.2341_2344del, NR_038306.1:n.2342_2344del, NR_038306.1:n.2343_2344del, NR_038306.1:n.2344del, NR_038306.1:n.2344dup, NR_038306.1:n.2343_2344dup, NR_038306.1:n.2342_2344dup, NR_038306.1:n.2341_2344dup, NR_038306.1:n.2340_2344dup, NR_038306.1:n.2339_2344dup, NR_038306.1:n.2344_2345insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NR_038307.1:n.2314_2329del, NR_038307.1:n.2315_2329del, NR_038307.1:n.2316_2329del, NR_038307.1:n.2318_2329del, NR_038307.1:n.2319_2329del, NR_038307.1:n.2320_2329del, NR_038307.1:n.2321_2329del, NR_038307.1:n.2322_2329del, NR_038307.1:n.2325_2329del, NR_038307.1:n.2326_2329del, NR_038307.1:n.2327_2329del, NR_038307.1:n.2328_2329del, NR_038307.1:n.2329del, NR_038307.1:n.2329dup, NR_038307.1:n.2328_2329dup, NR_038307.1:n.2327_2329dup, NR_038307.1:n.2326_2329dup, NR_038307.1:n.2325_2329dup, NR_038307.1:n.2324_2329dup, NR_038307.1:n.2329_2330insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NR_038308.1:n.2275_2290del, NR_038308.1:n.2276_2290del, NR_038308.1:n.2277_2290del, NR_038308.1:n.2279_2290del, NR_038308.1:n.2280_2290del, NR_038308.1:n.2281_2290del, NR_038308.1:n.2282_2290del, NR_038308.1:n.2283_2290del, NR_038308.1:n.2286_2290del, NR_038308.1:n.2287_2290del, NR_038308.1:n.2288_2290del, NR_038308.1:n.2289_2290del, NR_038308.1:n.2290del, NR_038308.1:n.2290dup, NR_038308.1:n.2289_2290dup, NR_038308.1:n.2288_2290dup, NR_038308.1:n.2287_2290dup, NR_038308.1:n.2286_2290dup, NR_038308.1:n.2285_2290dup, NR_038308.1:n.2290_2291insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

                    10.

                    rs1491034974 has merged into rs1553905111 [Homo sapiens]
                      Variant type:
                      DELINS
                      Alleles:
                      GTGTGTGT>-,GT,GTGT,GTGTGT,GTGTGTGTGT,GTGTGTGTGTGT,GTGTGTGTGTGTGT [Show Flanks]
                      Chromosome:
                      4:78666761 (GRCh38)
                      4:79587915 (GRCh37)
                      Canonical SPDI:
                      NC_000004.12:78666743:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGT,NC_000004.12:78666743:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGT,NC_000004.12:78666743:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGT,NC_000004.12:78666743:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGT,NC_000004.12:78666743:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000004.12:78666743:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000004.12:78666743:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT
                      Gene:
                      LINC01094 (Varview)
                      Functional Consequence:
                      intron_variant
                      Validated:
                      by frequency,by alfa,by cluster
                      MAF:
                      TGTGTGTGTGTGTGTGTGT=0./0 (ALFA)
                      -=0.00167/1 (NorthernSweden)
                      -=0.00548/10 (Korea1K)
                      TG=0.38188/1416 (TWINSUK)
                      TG=0.38921/1500 (ALSPAC)
                      HGVS:

                      11.

                      rs1490777525 [Homo sapiens]
                        Variant type:
                        SNV
                        Alleles:
                        C>A [Show Flanks]
                        Chromosome:
                        4:78670623 (GRCh38)
                        4:79591777 (GRCh37)
                        Canonical SPDI:
                        NC_000004.12:78670622:C:A
                        Gene:
                        LINC01094 (Varview)
                        Functional Consequence:
                        intron_variant
                        Validated:
                        by frequency,by alfa
                        MAF:
                        A=0./0 (ALFA)
                        HGVS:

                        12.

                        rs1490644165 [Homo sapiens]
                          Variant type:
                          SNV
                          Alleles:
                          A>C [Show Flanks]
                          Chromosome:
                          4:78656529 (GRCh38)
                          4:79577683 (GRCh37)
                          Canonical SPDI:
                          NC_000004.12:78656528:A:C
                          Gene:
                          LINC01094 (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:

                          13.

                          rs1490643121 [Homo sapiens]
                            Variant type:
                            SNV
                            Alleles:
                            C>T [Show Flanks]
                            Chromosome:
                            4:78671307 (GRCh38)
                            4:79592461 (GRCh37)
                            Canonical SPDI:
                            NC_000004.12:78671306:C:T
                            Gene:
                            LINC01094 (Varview)
                            Functional Consequence:
                            intron_variant
                            Validated:
                            by frequency,by alfa,by cluster
                            MAF:
                            T=0./0 (ALFA)
                            T=0.000014/2 (GnomAD)
                            T=0.000019/5 (TOPMED)
                            HGVS:

                            14.

                            rs1490384092 [Homo sapiens]
                              Variant type:
                              SNV
                              Alleles:
                              C>T [Show Flanks]
                              Chromosome:
                              4:78678921 (GRCh38)
                              4:79600075 (GRCh37)
                              Canonical SPDI:
                              NC_000004.12:78678920:C:T
                              Gene:
                              LINC01094 (Varview)
                              Functional Consequence:
                              intron_variant
                              Validated:
                              by frequency,by alfa
                              MAF:
                              T=0.000084/1 (ALFA)
                              T=0.000022/3 (GnomAD)
                              HGVS:

                              15.

                              rs1490359117 [Homo sapiens]
                                Variant type:
                                SNV
                                Alleles:
                                A>G,T [Show Flanks]
                                Chromosome:
                                4:78663149 (GRCh38)
                                4:79584303 (GRCh37)
                                Canonical SPDI:
                                NC_000004.12:78663148:A:G,NC_000004.12:78663148:A:T
                                Gene:
                                LINC01094 (Varview)
                                Functional Consequence:
                                intron_variant
                                Validated:
                                by frequency,by alfa,by cluster
                                MAF:
                                G=0./0 (ALFA)
                                G=0.000004/1 (TOPMED)
                                T=0.000035/1 (TOMMO)
                                HGVS:

                                16.

                                rs1490336544 [Homo sapiens]
                                  Variant type:
                                  SNV
                                  Alleles:
                                  A>T [Show Flanks]
                                  Chromosome:
                                  4:78673308 (GRCh38)
                                  4:79594462 (GRCh37)
                                  Canonical SPDI:
                                  NC_000004.12:78673307:A:T
                                  Gene:
                                  LINC01094 (Varview)
                                  Functional Consequence:
                                  intron_variant
                                  Validated:
                                  by frequency,by alfa,by cluster
                                  MAF:
                                  T=0./0 (ALFA)
                                  T=0.000004/1 (TOPMED)
                                  T=0.000007/1 (GnomAD)
                                  HGVS:

                                  17.

                                  rs1490198916 [Homo sapiens]
                                    Variant type:
                                    SNV
                                    Alleles:
                                    C>T [Show Flanks]
                                    Chromosome:
                                    4:78652037 (GRCh38)
                                    4:79573191 (GRCh37)
                                    Canonical SPDI:
                                    NC_000004.12:78652036:C:T
                                    Gene:
                                    LINC01094 (Varview)
                                    Functional Consequence:
                                    intron_variant
                                    Validated:
                                    by frequency,by alfa,by cluster
                                    MAF:
                                    T=0./0 (ALFA)
                                    T=0.000007/1 (GnomAD)
                                    T=0.000008/2 (TOPMED)
                                    HGVS:

                                    18.

                                    rs1490081368 [Homo sapiens]
                                      Variant type:
                                      SNV
                                      Alleles:
                                      T>C,G [Show Flanks]
                                      Chromosome:
                                      4:78665400 (GRCh38)
                                      4:79586554 (GRCh37)
                                      Canonical SPDI:
                                      NC_000004.12:78665399:T:C,NC_000004.12:78665399:T:G
                                      Gene:
                                      LINC01094 (Varview)
                                      Functional Consequence:
                                      intron_variant
                                      Validated:
                                      by frequency,by alfa,by cluster
                                      MAF:
                                      G=0./0 (ALFA)
                                      C=0.000007/1 (GnomAD)
                                      HGVS:

                                      19.

                                      rs1490042790 [Homo sapiens]
                                        Variant type:
                                        SNV
                                        Alleles:
                                        T>C [Show Flanks]
                                        Chromosome:
                                        4:78648852 (GRCh38)
                                        4:79570006 (GRCh37)
                                        Canonical SPDI:
                                        NC_000004.12:78648851:T:C
                                        Gene:
                                        LINC01094 (Varview)
                                        Functional Consequence:
                                        intron_variant
                                        Validated:
                                        by frequency,by alfa
                                        MAF:
                                        C=0./0 (ALFA)
                                        C=0.000011/3 (TOPMED)
                                        HGVS:

                                        20.

                                        rs1489919653 [Homo sapiens]
                                          Variant type:
                                          SNV
                                          Alleles:
                                          T>C,G [Show Flanks]
                                          Chromosome:
                                          4:78671549 (GRCh38)
                                          4:79592703 (GRCh37)
                                          Canonical SPDI:
                                          NC_000004.12:78671548:T:C,NC_000004.12:78671548:T:G
                                          Gene:
                                          LINC01094 (Varview)
                                          Functional Consequence:
                                          intron_variant
                                          HGVS:

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