RS5030858 PAH
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What This Variant Does
"rs5030858, also known as Arg408Trp or R408W, is a SNP in the phenylalanine hydroxylase PAH gene on c...
Associated Conditions
Phenylketonuria
PAH-related disorder
Inborn genetic diseases
See cases
Phenylketonuria
PAH-related disorder
Inborn genetic diseases
See cases
GWAS Studies (1)
| Trait | Risk Allele | OR / Beta | P-value | Study |
|---|---|---|---|---|
| Phenylalanine levels | G | OR: 1.55 | 4E-198 | PubMed |
Other Variants in PAH