rs137852231(A;A)

common in clinvar

Is a	genotype
of	rs137852231
Gene	F9
Chromosome	X
Position	139,541,085
mentioned	by

Magnitude

0

Repute

Good

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