Links from MedGen
Items: 4
| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 21 +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Autosomal dominant nonsyndromic hearing loss 21 +3 more | |
| | | Deletion (inframe_deletion) | not provided | |
| | | Single nucleotide variant (intron variant) | Autosomal recessive nonsyndromic hearing loss 104 +3 more | |
Click to view in NCBI Gene