rs137852259(G;G)

common in clinvar

Is a	genotype
of	rs137852259
Gene	F9
Chromosome	X
Position	139,561,821
mentioned	by

Magnitude

0

Repute

Good

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