rs137852269(T;T)

common in clinvar

Is a	genotype
of	rs137852269
Gene	F9
Chromosome	X
Position	139,562,042
mentioned	by

Magnitude

0

Repute

Good

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