RS1589451049 PSAP

Health Risk Chr 10:71828158
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Associated Conditions
Sphingolipid activator protein 1 deficiency
Parkinson disease 24
autosomal dominant
susceptibility to
Sphingolipid activator protein 1 deficiency
Parkinson disease 24
autosomal dominant
susceptibility to
Other Variants in PSAP
rs121918103 rs759960679 rs121918104 rs121918105 rs121918106 rs121918107 rs1842310280 rs121918108 rs121918109 rs121918110
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