rs137852271(G;G)

common in clinvar

Is a	genotype
of	rs137852271
Gene	F9
Chromosome	X
Position	139,561,805
mentioned	by

Magnitude

0

Repute

Good

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