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1.

rs190741280 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    G>A,T [Show Flanks]
    Chromosome:
    1:55509540 (GRCh38)
    1:55975213 (GRCh37)
    Canonical SPDI:
    NC_000001.11:55509539:G:A,NC_000001.11:55509539:G:T
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    A=0.000418/6 (ALFA)
    A=0.002396/12 (1000Genomes)
    A=0.003619/958 (TOPMED)
    HGVS:

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