RS587779388 AP4B1

Health Risk Chr 1:113898755
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What This Variant Does
"CLNSIG=5
Associated Conditions
Hereditary spastic paraplegia 47
Inborn genetic diseases
Intellectual disability
Abnormality of the nervous system
Spastic paraplegia
Hereditary spastic paraplegia 47
Inborn genetic diseases
Intellectual disability
Abnormality of the nervous system
Spastic paraplegia
Other Variants in AP4B1
rs587783179 rs376478015 rs797045244 rs200301524 rs879255397 rs879255396 rs746890435 rs141417436 rs1060499756 rs1060499771
Ask Dr. Hemsworth about this variant