rs104894844(G;G)

common in clinvar

Is a	genotype
of	rs104894844
Gene	GLA, RPL36A-HNRNPH2
Chromosome	X
Position	101,397,907
mentioned	by

Magnitude

0

Repute

Good

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