| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (nonsense) | Autosomal recessive nonsyndromic hearing loss 25 +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | GRXCR1-related condition +3 more | |
Click to view in NCBI Gene