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rs63749818(C;C)

From SNPedia
common in clinvar
Is agenotype
ofrs63749818
GeneMLH1
Chromosome3
Position37,007,002
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(A;C) 6 Lynch syndrome, pathogenic mutation
(C;C) 0 common in clinvar
(C;G) 6 Lynch syndrome