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1.

rs4480378 has merged into rs4001578 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    A>C,G [Show Flanks]
    Chromosome:
    1:83360033 (GRCh38)
    1:83825716 (GRCh37)
    Canonical SPDI:
    NC_000001.11:83360032:A:C,NC_000001.11:83360032:A:G
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    A=0.338034/6017 (ALFA)
    A=0.175764/322 (Korea1K)
    A=0.17757/38 (Vietnamese)
    A=0.17884/524 (KOREAN)
    A=0.183578/1328 (Korea4K)
    A=0.187048/14470 (TOMMO)
    A=0.196154/102 (SGDP_PRJ)
    A=0.225309/73 (HapMap)
    A=0.23913/11 (Siberian)
    A=0.25/54 (Qatari)
    A=0.265147/1698 (1000Genomes_30X)
    A=0.266773/1336 (1000Genomes)
    A=0.296838/78570 (TOPMED)
    A=0.297595/297 (GoNL)
    A=0.304865/45417 (GnomAD_genomes)
    A=0.344318/1327 (ALSPAC)
    A=0.355/213 (NorthernSweden)
    A=0.357875/1327 (TWINSUK)
    A=0.4/16 (GENOME_DK)
    HGVS:

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