RS770285398 CYP7B1

Health Risk Chr 8:64616217
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What This Variant Does
"CLNSIG=5
Associated Conditions
Spastic paraplegia
Inborn genetic diseases
Hereditary spastic paraplegia 5A
Congenital bile acid synthesis defect 3
Spastic paraplegia
Inborn genetic diseases
Hereditary spastic paraplegia 5A
Congenital bile acid synthesis defect 3
Other Variants in CYP7B1
rs72554620 rs121908610 rs121908614 rs121908611 rs121908612 rs121908613 rs267606758 rs116171274 rs267601966 rs587777222
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