RS121918107 PSAP

Health Risk Chr 10:71828091
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What This Variant Does
"[OMIM:?]
Associated Conditions
Sphingolipid activator protein 1 deficiency
PSAP-related disorder
Metachromatic leukodystrophy
Sphingolipid activator protein 1 deficiency
PSAP-related disorder
Metachromatic leukodystrophy
Other Variants in PSAP
rs121918103 rs759960679 rs121918104 rs121918105 rs121918106 rs1589451049 rs1842310280 rs121918108 rs121918109 rs121918110
Ask Dr. Hemsworth about this variant