rs786204841(A;G)
From SNPedia
| Carrier of a deafness mutation |
| Is a | genotype |
| of | rs786204841 |
| Gene | CLDN14, LOC105369301 |
| Chromosome | 21 |
| Position | 36,461,002 |
| mentioned | by |
| Magnitude | 3 |
| Repute | Bad |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 6 | Deafness; early-onset (prelingual) |
| (A;G) | 3 | Carrier of a deafness mutation |
| (G;G) | 0 | common in clinvar |
Unaffected in absence of a second mutation; see rs786204841.
