RS879255396 AP4B1

Health Risk Chr 1:113902864
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What This Variant Does
"CLNSIG=5
Associated Conditions
Spastic paraplegia
Hereditary spastic paraplegia 47
Hereditary spastic paraplegia 47
Spastic paraplegia
Inborn genetic diseases
Spastic paraplegia
Hereditary spastic paraplegia 47
Hereditary spastic paraplegia 47
Spastic paraplegia
Inborn genetic diseases
Other Variants in AP4B1
rs587779388 rs587783179 rs376478015 rs797045244 rs200301524 rs879255397 rs746890435 rs141417436 rs1060499756 rs1060499771
Ask Dr. Hemsworth about this variant