Unknown
| Variant Name | Allele Count | Allele Frequency | Associated Disease | Associated Gene |
|---|---|---|---|---|
| NM_001292063.2:c.1214C>A | 1 | |||
| NM_001378457.1:c.796C>T | 1 |
| Subject Id | Country | HPO Terms | Sex | Family History | Parental Consanguinity | Remarks |
|---|---|---|---|---|---|---|
| 604487.2 | United Arab Emirates | Hearing impairment | Unknown | Patient has heterozygous variants in OTOG, MYO7A and OTOA. All three of these genes are hearing loss-associated. |