G2Cdb::Allele report
- Mutation type
- N
Altered genes (1)
| Gene | Symbol | Species | Description |
|---|---|---|---|
| G00001821 | SHANK2 | Homo sapiens | SH3 and multiple ankyrin repeat domains 2 |
Diseases (1)
| Disease | Description | Nervous effect |
|---|---|---|
| D00000220 | Hearing impairment (autosomal recessive nonsyndromic) | Y |