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

i5006379

From SNPedia
23andMe dataI5006379
23andMe searchI5006379
opensnpI5006379
Gene (via rs)VHL
aliasrs104893831
Rs_StabilizedOrientationplus
RsGeno Mag Summary
(G;G) 0 common in clinvar
(G;T) 7 Von Hippel-Lindau syndrome mutation

rs104893831

Retrieved from "https://www.SNPedia.com/index.php?title=I5006379&oldid=1615375"
Powered by MediaWiki
Powered by Semantic MediaWiki
Powered by the NCBI