rs1799989(A;C)
From SNPedia
| benign most likely |
| Is a | genotype |
| of | rs1799989 |
| Gene | TYR, LOC107984363 |
| Chromosome | 11 |
| Position | 89,177,755 |
| mentioned | by |
| Magnitude | 0.5 |
| Repute | Bad |
| Geno | Mag | Summary |
|---|---|---|
| (A;C) | 0.5 | benign most likely |
| (C;C) | 0 | common in clinvar |
although reported as an albinism allele, the frequency of this variant seems far too high in most populations to give credence to this.
