rs137852469(G;G)

common in clinvar

Is a	genotype
of	rs137852469
Gene	F8
Chromosome	X
Position	154,860,588
Merged from	Rs28937307
mentioned	by

Magnitude

0

Repute

Good

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