rs118203925(T;T)
From SNPedia
Non-phenylketonuria hyperphenylalaninemia genotype |
Is a | genotype |
of | rs118203925 |
Gene | PAH |
Chromosome | 12 |
Position | 102,912,819 |
mentioned | by |
Magnitude | 5.9 |
Repute | Bad |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
(C;T) | 3 | Carrier of a non-phenylketonuria hyperphenylalaninemia allele |
(T;T) | 5.9 | Non-phenylketonuria hyperphenylalaninemia genotype |
see hyperphenylalaninemia and the ClinVar link on the SNP page for this SNP