Links from MedGen
Items: 2
| Gene(s) | Protein change | Condition(s) | Clinical significance
(Last reviewed) | Review status |
|---|
| - GRCh37:
- Chr7:129414596
- GRCh38:
- Chr7:129774756
| MIR96 | | Autosomal dominant nonsyndromic hearing loss 50 | Pathogenic
(May 1, 2009) | no assertion criteria provided |
| - GRCh37:
- Chr7:129414597
- GRCh38:
- Chr7:129774757
| MIR96 | | Autosomal dominant nonsyndromic hearing loss 50 | Pathogenic
(May 1, 2009) | no assertion criteria provided |