RS104894827 GLA

Health Risk Chr X:101398033
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What This Variant Does
"The rare minor allele of this variant is reported to be pathogenic/likely pathogenic for familial hy...
Associated Conditions
Fabry disease
GLA-related disorder
Fabry disease
GLA-related disorder
Other Variants in GLA
rs104894828 rs104894829 rs104894830 rs104894831 rs1603038103 rs28935485 rs104894832 rs104894833 rs104894835 rs104894836
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