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1.

rs1802743 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    C>A [Show Flanks]
    Chromosome:
    12:91104245 (GRCh38)
    12:91498022 (GRCh37)
    Canonical SPDI:
    NC_000012.12:91104244:C:A
    Gene:
    LUM (Varview)
    Functional Consequence:
    missense_variant,coding_sequence_variant
    HGVS:

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