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1.

rs2430561 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    T>A,G [Show Flanks]
    Chromosome:
    12:68158742 (GRCh38)
    12:68552522 (GRCh37)
    Canonical SPDI:
    NC_000012.12:68158741:T:A,NC_000012.12:68158741:T:G
    Gene:
    IFNG (Varview)
    Functional Consequence:
    intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    A=0.39991/7136 (ALFA)
    A=0.043689/162 (TWINSUK)
    A=0.054489/210 (ALSPAC)
    A=0.06513/65 (GoNL)
    A=0.105864/8193 (TOMMO)
    A=0.11514/832 (Korea4K)
    A=0.128337/375 (KOREAN)
    A=0.259867/20451 (PAGE_STUDY)
    A=0.275141/1762 (1000Genomes_30X)
    A=0.280152/1403 (1000Genomes)
    T=0.320144/89 (SGDP_PRJ)
    A=0.352325/93257 (TOPMED)
    A=0.360837/53536 (GnomAD_genomes)
    T=0.4/12 (Siberian)
    A=0.468333/281 (NorthernSweden)
    A=0.481481/104 (Qatari)
    T=0.5/20 (GENOME_DK)
    HGVS:

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