rs786200861(-;TCT)
From SNPedia
| Carrier of a phenylketonuria mutation |
| Is a | genotype |
| of | rs786200861 |
| Gene | PAH |
| Chromosome | 12 |
| Position | 102,843,751 |
| Merged into | Rs62516096 |
| mentioned | by |
| Magnitude | 3 |
| Repute | Bad |
| Geno | Mag | Summary |
|---|---|---|
| (-;TCT) | 3 | Carrier of a phenylketonuria mutation |
| (TCT;TCT) | 0 | common in clinvar |
Phenylketonuria mutation carrier; unaffected unless a second PKU mutation is present.
