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1.

rs2464171 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    A>G [Show Flanks]
    Chromosome:
    12:91051183 (GRCh38)
    12:91444960 (GRCh37)
    Canonical SPDI:
    NC_000012.12:91051182:A:G
    Gene:
    KERA (Varview)
    Functional Consequence:
    3_prime_UTR_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    G=0./0 (ALFA)
    G=0.000004/1 (TOPMED)
    G=0.00641/2 (HapMap)
    HGVS:

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