rs11090865(T;T)
From SNPedia
| Modifier variant; some impact in rare cases |
| Is a | genotype |
| of | rs11090865 |
| Gene | TRMU |
| Chromosome | 22 |
| Position | 46,335,792 |
| mentioned | by |
| Magnitude | 3 |
| Repute | Bad |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| (G;T) | 2.3 | Carrier of a deafness-related modifier variant |
| (T;T) | 3 | Modifier variant; some impact in rare cases |
See text on main rs-page
