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

rs267607944(G;G)

From SNPedia

Jump to:navigation, search

common in clinvar

Is a	genotype
of	rs267607944
Gene	MSH2
Chromosome	2
Position	47,429,741
mentioned	by

0

Good

Geno	Mag	Summary
(C;G)	6	Likely miscall in Ancestry data; otherwise, Lynch syndrome, pathogenic mutation
(G;G)	0	common in clinvar
(G;T)	6	Lynch syndrome, pathogenic mutation

Retrieved from "https://www.SNPedia.com/index.php?title=Rs267607944(G;G)&oldid=724247"

Is a genotype