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

rs398123217(A;A)

From SNPedia
common in clinvar
Is agenotype
ofrs398123217
GeneGLA, RPL36A-HNRNPH2
ChromosomeX
Position101,398,939
mentionedby
Magnitude0
ReputeGood
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