rs137852235(G;G)

common in clinvar

Is a	genotype
of	rs137852235
Gene	F9
Chromosome	X
Position	139,548,450
mentioned	by

Magnitude

0

Repute

Good

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