RS876661295 AP4S1

Health Risk Chr 14:31066333
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What This Variant Does
"CLNSIG=5
Associated Conditions
Hereditary spastic paraplegia 52
APS41-related disorder
Intellectual disability
Neurodevelopmental disorder
Spastic paraplegia
Inborn genetic diseases
Hereditary spastic paraplegia 52
APS41-related disorder
Intellectual disability
Neurodevelopmental disorder
Spastic paraplegia
Inborn genetic diseases
Other Variants in AP4S1
rs2139067616 rs200033849 rs2139569112 rs758748011 rs2139067696 rs1566532837 rs777974629 rs2502388612 rs2502522773 rs563687343
Ask Dr. Hemsworth about this variant