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rs386829069(C;C)

From SNPedia
Likely miscall if from Ancestry data; otherwise, Leigh syndrome mutation
Is agenotype
ofrs386829069
GeneATP6
ChromosomeMT
Position9,191
Merged fromRs397507451
mentionedby
Magnitude3
ReputeBad
Geno Mag Summary
(C;C) 3 Likely miscall if from Ancestry data; otherwise, Leigh syndrome mutation
(T;T) 0 common in clinvar

Seen too often in Ancestry v2 data compared to reported frequency worldwide, so likely to be a miscall in data from Ancestry. If your data is not from Ancestry, let us know.