rs35887622(G;G)
From SNPedia
| Variant of unclear significance wrt deafness |
| Is a | genotype |
| of | rs35887622 |
| Gene | GJB2 |
| Chromosome | 13 |
| Position | 20,189,481 |
| mentioned | by |
| Magnitude | 3 |
| Repute | Bad |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | normal hearing |
| (A;C) | 3 | Carrier of a recessive deafness mutation |
| (A;G) | 3 | Variant of unclear significance wrt deafness |
| (G;G) | 3 | Variant of unclear significance wrt deafness |
see discussion at rs35887622
