Have questions? Visit https://www.reddit.com/r/SNPedia

rs104894827(C;T)

From SNPedia
Carrier of a Fabry disease mutation; X-linked so risk is to sons
Is agenotype
ofrs104894827
GeneGLA, RPL36A-HNRNPH2
ChromosomeX
Position101,398,033
mentionedby
Magnitude3
ReputeBad
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

Mostly unaffected in absence of a second GLA gene mutation; see text and links via main rs-page