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

i5037863

From SNPedia
23andMe dataI5037863
23andMe searchI5037863
opensnpI5037863
Gene (via rs)MSH6
aliasrs267608056
Rs_StabilizedOrientationplus
RsGeno Mag Summary
(-;C) 6 Lynch syndrome, pathogenic mutation
(C;C) 0 common in clinvar

rs267608056

Retrieved from "https://bots.SNPedia.com/index.php?title=I5037863&oldid=1519579"
Powered by MediaWiki
Powered by Semantic MediaWiki
Powered by the NCBI