Unknown
| Variant Name | Allele Count | Allele Frequency | Associated Disease | Associated Gene |
|---|---|---|---|---|
| NM_153676.4:c.121G>A | 1 | |||
| NM_004999.4:c.3019C>T | 1 |
| Subject Id | Country | HPO Terms | Sex | Family History | Parental Consanguinity | Remarks |
|---|---|---|---|---|---|---|
| 600970.2 | United Arab Emirates | Hearing impairment | Unknown | Patient has heterozygous variants in MYO6 and LOXHD1. Both of these genes are hearing loss-associated. |