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rs104894841(C;C)

From SNPedia
common in clinvar
Is agenotype
ofrs104894841
GeneGLA, RPL36A-HNRNPH2
ChromosomeX
Position101,398,907
mentionedby
Magnitude0
ReputeGood
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