rs137852246(T;T)

common in clinvar

Is a	genotype
of	rs137852246
Gene	F9
Chromosome	X
Position	139,560,821
mentioned	by

Magnitude

0

Repute

Good

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