RS140066253 PSAP

Health Risk Chr 10:71819818
Upload your DNA to see your genotype for this variant.
Associated Conditions
Gaucher disease due to saposin C deficiency
Combined PSAP deficiency
Sphingolipid activator protein 1 deficiency
Krabbe disease due to saposin A deficiency
Metachromatic leukodystrophy
Gaucher disease due to saposin C deficiency
Combined PSAP deficiency
Sphingolipid activator protein 1 deficiency
Krabbe disease due to saposin A deficiency
Metachromatic leukodystrophy
Other Variants in PSAP
rs121918103 rs759960679 rs121918104 rs121918105 rs121918106 rs1589451049 rs121918107 rs1842310280 rs121918108 rs121918109
Ask Dr. Hemsworth about this variant