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1.

rs1000000038 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    C>T [Show Flanks]
    Chromosome:
    8:62587167 (GRCh38)
    8:63499726 (GRCh37)
    Canonical SPDI:
    NC_000008.11:62587166:C:T
    Gene:
    NKAIN3 (Varview)
    Functional Consequence:
    intron_variant
    Validated:
    by frequency,by alfa
    MAF:
    T=0./0 (ALFA)
    HGVS:

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