rs111033367(-;CT)
From SNPedia
| Carrier of an Usher syndrome type 2A mutation |
| Is a | genotype |
| of | rs111033367 |
| Gene | USH2A |
| Chromosome | 1 |
| Position | 216,190,280 |
| mentioned | by |
| Magnitude | 3 |
| Repute | Bad |
| Geno | Mag | Summary |
|---|---|---|
| (-;-) | 5 | Usher syndrome, type 2A |
| (CT;CT) | 0 | common in clinvar |
Unaffected in absence of a second mutation in the USH2A gene; see links via main rs-page.
