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1.

rs8036042 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    G>A [Show Flanks]
    Chromosome:
    15:78471982 (GRCh38)
    15:78764324 (GRCh37)
    Canonical SPDI:
    NC_000015.10:78471981:G:A
    Gene:
    IREB2 (Varview)
    Functional Consequence:
    intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    A=0.156212/3561 (ALFA)
    A=0.100341/294 (KOREAN)
    A=0.103166/189 (Korea1K)
    A=0.11215/24 (Vietnamese)
    A=0.124106/2080 (TOMMO)
    A=0.125/5 (GENOME_DK)
    A=0.125468/67 (MGP)
    A=0.141006/706 (1000Genomes)
    A=0.145948/38631 (TOPMED)
    A=0.149686/20968 (GnomAD)
    A=0.151303/151 (GoNL)
    A=0.152902/685 (Estonian)
    A=0.163726/631 (ALSPAC)
    A=0.164509/610 (TWINSUK)
    A=0.165/99 (NorthernSweden)
    A=0.189815/41 (Qatari)
    G=0.45/81 (SGDP_PRJ)
    G=0.5/3 (Siberian)
    HGVS:

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