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rs267607720(C;C)

From SNPedia
common in clinvar
Is agenotype
ofrs267607720
GeneMLH1
Chromosome3
Position37,000,952
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(C;C) 0 common in clinvar
(C;G) 6 Likely miscall in v5 23andMe data or v2 Ancestry data; otherwise, Lynch syndrome, pathogenic mutation
(C;T) 6 Lynch syndrome