rs121918166(A;G)
From SNPedia
| Carrier of an oculocutaneous Albinism Type II mutation |
| Is a | genotype |
| of | rs121918166 |
| Gene | OCA2 |
| Chromosome | 15 |
| Position | 27,985,101 |
| Merged from | Rs28934272 |
| mentioned | by |
| Magnitude | 3 |
| Repute | Bad |
| Geno | Mag | Summary |
|---|---|---|
| (A;G) | 3 | Carrier of an oculocutaneous Albinism Type II mutation |
| (G;G) | 0 | common in clinvar |
Unaffected unless carrying another pathogenic OCA2 gene mutation
