RS104894828 GLA

Health Risk Chr X:101398467
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What This Variant Does
"[OMIM:?]
Associated Conditions
Fabry disease
cardiac variant
Cardiovascular phenotype
Primary familial hypertrophic cardiomyopathy
Fabry disease
Fabry disease
Fabry disease
cardiac variant
Cardiovascular phenotype
Primary familial hypertrophic cardiomyopathy
Fabry disease
Fabry disease
Other Variants in GLA
rs104894827 rs104894829 rs104894830 rs104894831 rs1603038103 rs28935485 rs104894832 rs104894833 rs104894835 rs104894836
Ask Dr. Hemsworth about this variant