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2.

rs2036787640 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    G>C [Show Flanks]
    Chromosome:
    13:42875512 (GRCh38)
    13:43449648 (GRCh37)
    Canonical SPDI:
    NC_000013.11:42875511:G:C
    Validated:
    by frequency,by alfa
    MAF:
    C=0./0 (ALFA)
    C=0.000004/1 (TOPMED)
    HGVS:

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