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1.

rs2235961 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    G>A [Show Flanks]
    Chromosome:
    14:54396859 (GRCh38)
    14:54863577 (GRCh37)
    Canonical SPDI:
    NC_000014.9:54396858:G:A
    Gene:
    CDKN3 (Varview)
    Functional Consequence:
    2KB_upstream_variant,upstream_transcript_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    G=0.282508/74490 (ALFA)
    G=0.227273/105 (SGDP_PRJ)
    G=0.262325/1011 (ALSPAC)
    G=0.268519/58 (Qatari)
    G=0.269687/1000 (TWINSUK)
    G=0.286573/286 (GoNL)
    G=0.286581/75855 (TOPMED)
    G=0.288462/15 (Siberian)
    G=0.290119/84018 (GnomAD_exomes)
    G=0.290179/1300 (Estonian)
    G=0.290766/43362 (GnomAD_genomes)
    G=0.306554/580 (HapMap)
    G=0.308166/24249 (PAGE_STUDY)
    G=0.31269/24216 (TOMMO)
    G=0.314103/245 (PRJEB37584)
    G=0.31574/2022 (1000Genomes_30X)
    G=0.316094/1583 (1000Genomes)
    G=0.31714/581 (Korea1K)
    G=0.329046/2379 (Korea4K)
    G=0.332082/973 (KOREAN)
    G=0.35/14 (GENOME_DK)
    G=0.373333/224 (NorthernSweden)
    G=0.383178/82 (Vietnamese)
    HGVS:

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