| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Duplication (intron variant) | GNAQ-related disorder | |
| | | Single nucleotide variant (intron variant) | GNAQ-related disorder | |
| | | Deletion (intron variant) | GNAQ-related disorder | |
| | | Single nucleotide variant (missense variant) | GNAQ-related disorder | |
Click to view in NCBI Gene