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

rs137852451(C;C)

From SNPedia

Jump to:navigation, search

common in clinvar

Is a	genotype
of	rs137852451
Gene	F8
Chromosome	X
Position	154,903,966
Merged from	Rs28937297
mentioned	by

0

Good

Geno	Mag	Summary
(C;C)	0	common in clinvar
(C;T)	3.5	Carrier of a Hemophilia A mutation
(T;T)	5.5	Hemophilia A (severity varies)

Retrieved from "https://www.SNPedia.com/index.php?title=Rs137852451(C;C)&oldid=510640"

Is a genotype