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1.

rs1409398230 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    G>A,T [Show Flanks]
    Chromosome:
    1:55523121 (GRCh38)
    1:55988794 (GRCh37)
    Canonical SPDI:
    NC_000001.11:55523120:G:A,NC_000001.11:55523120:G:T
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    T=0./0 (ALFA)
    HGVS:

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