RS76212747 PAH
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
Hyperphenylalaninemia
Phenylketonuria
Inborn genetic diseases
Phenylketonuria
Hyperphenylalaninemia
Phenylketonuria
Inborn genetic diseases
Phenylketonuria
Other Variants in PAH