RS104894845 GLA

Health Risk Chr X:101401752
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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
Cardiomyopathy
Cardiovascular phenotype
GLA-related disorder
Fabry disease
Cardiovascular phenotype
Fabry disease
Cardiomyopathy
Cardiovascular phenotype
GLA-related disorder
Fabry disease
Cardiovascular phenotype
Other Variants in GLA
rs104894827 rs104894828 rs104894829 rs104894830 rs104894831 rs1603038103 rs28935485 rs104894832 rs104894833 rs104894835
Ask Dr. Hemsworth about this variant