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1.

rs5 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    C>T [Show Flanks]
    Chromosome:
    7:92209796 (GRCh38)
    7:91839110 (GRCh37)
    Canonical SPDI:
    NC_000007.14:92209795:C:T
    Gene:
    KRIT1 (Varview)
    Functional Consequence:
    intron_variant
    HGVS:

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