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rs104894835(A;A)

From SNPedia
common in clinvar
Is agenotype
ofrs104894835
GeneGLA, RPL36A-HNRNPH2, HNRNPH2
ChromosomeX
Position101,407,803
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