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1.

rs111033172 has merged into rs28358572 [Homo sapiens]
    ATAAACCCCGATCAACCTCACCACC[C/T]CTTGCTCAGCCTATATACCGCCATC
    Chromosome:
    MT:1243
    Allele Origin:
    T(germline)/C(germline)
    Clinical significance:
    Benign
    Validated:
    by cluster,by frequency
    HGVS:
    NC_012920.1:m.1243T>C

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