RS773556943 CCT5

Health Risk Chr 5:10254213
Upload your DNA to see your genotype for this variant.
Associated Conditions
Hereditary sensory and autonomic neuropathy with spastic paraplegia
CCT5-related disorder
Hereditary sensory and autonomic neuropathy with spastic paraplegia
CCT5-related disorder
Other Variants in CCT5
rs150870419 rs147989324 rs370529963 rs201171003 rs370943521 rs1281493996 rs542323956 rs925661175
Ask Dr. Hemsworth about this variant