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

rs778653296(C;C)

From SNPedia

Jump to:navigation, search

common in clinvar

Is a	genotype
of	rs778653296
Gene	HSPG2
Chromosome	1
Position	21,851,790
mentioned	by

0

Good

Geno	Mag	Summary
(A;A)	7.8	Schwartz Jampel syndrome type 1
(A;C)	3	Carrier for a Schwartz Jampel syndrome mutation
(C;C)	0	common in clinvar

Retrieved from "https://bots.SNPedia.com/index.php?title=Rs778653296(C;C)&oldid=1238976"

Is a genotype