RS62516092 PAH

Health Risk Chr 12:102844359
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Phenylketonuria
See cases
Inborn genetic diseases
PAH-related disorder
Phenylketonuria
See cases
Inborn genetic diseases
PAH-related disorder
Other Variants in PAH
rs5030861 rs5030858 rs62642936 rs62514959 rs62508698 rs76296470 rs5030849 rs62516151 rs5030847 rs62514891
Ask Dr. Hemsworth about this variant