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1.

rs1724894060 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    T>C [Show Flanks]
    Chromosome:
    3:197710904 (GRCh38)
    3:197437775 (GRCh37)
    Canonical SPDI:
    NC_000003.12:197710903:T:C
    Gene:
    RUBCN (Varview)
    Functional Consequence:
    intron_variant
    Validated:
    by frequency
    MAF:
    C=0.00006/1 (TOMMO)
    HGVS:

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