rs74486803(C;C)
From SNPedia
common in clinvar |
Is a | genotype |
of | rs74486803 |
Gene | PAH |
Chromosome | 12 |
Position | 102,855,315 |
mentioned | by |
Magnitude | 0 |
Repute | Good |
Geno | Mag | Summary |
---|---|---|
(A;A) | 5.9 | Non-phenylketonuria hyperphenylalaninemia genotype |
(A;C) | 3 | Carrier of a non-phenylketonuria hyperphenylalaninemia allele |
(C;C) | 0 | common in clinvar |
(C;T) | 3 | Carrier of a phenylketonuria mutation |