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

rs587776646(G;G)

From SNPedia

Jump to:navigation, search

common in clinvar

Is a	genotype
of	rs587776646
Gene	SDHD
Chromosome	11
Position	112,094,933
mentioned	by

0

Good

Geno	Mag	Summary
(-;G)	6.2	Hereditary PGL/PCC Syndrome
(G;G)	0	common in clinvar

Retrieved from "https://www.SNPedia.com/index.php?title=Rs587776646(G;G)&oldid=958932"

Is a genotype