RS797044499 GLA

Health Risk Chr X:101398569
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Fabry disease
Fabry disease
Cardiovascular phenotype
Fabry disease
Fabry disease
Cardiovascular phenotype
Other Variants in GLA
rs104894827 rs104894828 rs104894829 rs104894830 rs104894831 rs1603038103 rs28935485 rs104894832 rs104894833 rs104894835
Ask Dr. Hemsworth about this variant