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1.

rs199951903 [Homo sapiens]
    AACACTATTCTCACCAGACCTCCTA[A/G]GCGACCCAGACAATTATACCCTAGC
    Chromosome:
    MT:15497
    Gene:
    CYTB (GeneView)
    Functional Consequence:
    missense
    Allele Origin:
    G(germline)/A(germline)
    Clinical significance:
    other
    Validated:
    by cluster
    HGVS:
    NC_012920.1:m.15497G>A, YP_003024038.1:p.Gly251Ser

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