rs104894831(C;C)

common in clinvar

Is a	genotype
of	rs104894831
Gene	GLA, RPL36A-HNRNPH2, HNRNPH2
Chromosome	X
Position	101,407,786
mentioned	by

Magnitude

0

Repute

Good

Geno	Mag	Summary
(C;C)	0	common in clinvar
(C;T)	3	Carrier of a Fabry disease mutation; X-linked so risk is to sons
(T;T)	6	Fabry disease