RS121918104 PSAP

Health Risk Chr 10:71825892
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What This Variant Does
"[OMIM:?]
Associated Conditions
Sphingolipid activator protein 1 deficiency
Combined PSAP deficiency
Parkinson disease 24
autosomal dominant
susceptibility to
Sphingolipid activator protein 1 deficiency
Combined PSAP deficiency
Parkinson disease 24
autosomal dominant
susceptibility to
Other Variants in PSAP
rs121918103 rs759960679 rs121918105 rs121918106 rs1589451049 rs121918107 rs1842310280 rs121918108 rs121918109 rs121918110
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