RS28935197 GLA

Health Risk Chr X:101398942
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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
Cardiovascular phenotype
Hypertrophic cardiomyopathy
Cardiomyopathy
Fabry disease
Cardiovascular phenotype
Hypertrophic cardiomyopathy
Cardiomyopathy
Other Variants in GLA
rs104894827 rs104894828 rs104894829 rs104894830 rs104894831 rs1603038103 rs28935485 rs104894832 rs104894833 rs104894835
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