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1.

rs12861722 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    G>A [Show Flanks]
    Chromosome:
    13:58760950 (GRCh38)
    13:59335084 (GRCh37)
    Canonical SPDI:
    NC_000013.11:58760949:G:A
    Gene:
    LOC105370220 (Varview)
    Functional Consequence:
    intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    A=0.253097/4781 (ALFA)
    A=0.074766/16 (Vietnamese)
    A=0.120406/2018 (TOMMO)
    A=0.123891/363 (KOREAN)
    A=0.124454/228 (Korea1K)
    A=0.157407/34 (Qatari)
    A=0.157576/52 (HapMap)
    A=0.177316/888 (1000Genomes)
    A=0.225218/59613 (TOPMED)
    A=0.237154/33147 (GnomAD)
    A=0.254509/254 (GoNL)
    A=0.262675/974 (TWINSUK)
    A=0.266217/1026 (ALSPAC)
    A=0.295/177 (NorthernSweden)
    A=0.31942/1431 (Estonian)
    A=0.325/13 (GENOME_DK)
    G=0.4/12 (Siberian)
    G=0.414634/68 (SGDP_PRJ)
    HGVS:

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