rs104894835(A;A)

common in clinvar

Is a	genotype
of	rs104894835
Gene	GLA, RPL36A-HNRNPH2, HNRNPH2
Chromosome	X
Position	101,407,803
mentioned	by

Magnitude

0

Repute

Good

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