RS774088864 PSAP

Health Risk Chr 10:71819553
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Associated Conditions
Sphingolipid activator protein 1 deficiency
Inborn genetic diseases
Sphingolipid activator protein 1 deficiency
Inborn genetic diseases
Other Variants in PSAP
rs121918103 rs759960679 rs121918104 rs121918105 rs121918106 rs1589451049 rs121918107 rs1842310280 rs121918108 rs121918109
Ask Dr. Hemsworth about this variant