RS141507441 CPLANE1

Health Risk Chr 5:37125330
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Joubert syndrome 17
Orofaciodigital syndrome type 6
Inborn genetic diseases
Joubert syndrome 17
Orofaciodigital syndrome type 6
Inborn genetic diseases
Other Variants in CPLANE1
rs367543061 rs367543062 rs367543064 rs367543063 rs139675596 rs111294855 rs606231258 rs606231259 rs606231260 rs375009168
Ask Dr. Hemsworth about this variant