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1.

rs28376053 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    T>C [Show Flanks]
    Chromosome:
    4:20171706 (GRCh38)
    4:20173329 (GRCh37)
    Canonical SPDI:
    NC_000004.12:20171705:T:C
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    C=0.140012/3346 (ALFA)
    C=0.06869/43 (Chileans)
    C=0.115464/445 (ALSPAC)
    C=0.120208/602 (1000Genomes)
    C=0.12037/26 (Qatari)
    C=0.125547/804 (1000Genomes_30X)
    C=0.126483/469 (TWINSUK)
    C=0.143333/86 (NorthernSweden)
    C=0.14911/39468 (TOPMED)
    C=0.152009/681 (Estonian)
    C=0.152982/22802 (GnomAD_genomes)
    C=0.155311/155 (GoNL)
    C=0.193299/300 (HapMap)
    C=0.3/12 (GENOME_DK)
    T=0.394737/30 (SGDP_PRJ)
    T=0.5/5 (Siberian)
    HGVS:

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