rs137852467(C;C)

common in clinvar

Is a	genotype
of	rs137852467
Gene	F8
Chromosome	X
Position	154,863,113
Merged from	Rs28937304
mentioned	by

Magnitude

0

Repute

Good

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