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1.

rs2735334 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    A>G [Show Flanks]
    Chromosome:
    12:91056009 (GRCh38)
    12:91449786 (GRCh37)
    Canonical SPDI:
    NC_000012.12:91056008:A:G
    Gene:
    KERA (Varview)
    Functional Consequence:
    synonymous_variant,coding_sequence_variant
    HGVS:

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