Have questions? Visit https://www.reddit.com/r/SNPedia

rs63750611(C;C)

From SNPedia
common in clinvar
Is agenotype
ofrs63750611
GeneMSH2
Chromosome2
Position47,429,854
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 6 Lynch syndrome, pathogenic mutation