RS148833652 SPART

Health Risk Chr 13:36326691
Upload your DNA to see your genotype for this variant.
Associated Conditions
Troyer syndrome
Hereditary spastic paraplegia
Inborn genetic diseases
SPART-related disorder
Gastric cancer
Thyroid cancer
nonmedullary
1
Hepatocellular carcinoma
Lung cancer
Cervical cancer
Troyer syndrome
Hereditary spastic paraplegia
Inborn genetic diseases
SPART-related disorder
Other Variants in SPART
rs1060499524 rs775736341 rs730882198 rs146398746 rs148399669 rs140222511 rs368305530 rs149730980 rs571222120 rs370385005
Ask Dr. Hemsworth about this variant