| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (intron variant) | Joubert syndrome 30 | |
| | | Single nucleotide variant (synonymous variant +2 more) | not provided +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | Joubert syndrome 30 | |
| | | Single nucleotide variant (missense variant +1 more) | Joubert syndrome 30 | |
Click to view in NCBI Gene