RS377027316 PSAP

Health Risk Chr 10:71829044
Upload your DNA to see your genotype for this variant.
Associated Conditions
Sphingolipid activator protein 1 deficiency
Metachromatic leukodystrophy
Combined PSAP deficiency
PSAP-related disorder
Sphingolipid activator protein 1 deficiency
Metachromatic leukodystrophy
Combined PSAP deficiency
PSAP-related disorder
Other Variants in PSAP
rs121918103 rs759960679 rs121918104 rs121918105 rs121918106 rs1589451049 rs121918107 rs1842310280 rs121918108 rs121918109
Ask Dr. Hemsworth about this variant