| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Deletion (intron variant) | Bardet-Biedl syndrome 4 | |
| | | Single nucleotide variant (splice acceptor variant) | Bardet-Biedl syndrome 4 +1 more | |
| | | Single nucleotide variant (5 prime UTR variant +2 more) | Bardet-Biedl syndrome 4 | |
| | | Deletion (frameshift variant +1 more) | Bardet-Biedl syndrome +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (splice acceptor variant) | Bardet-Biedl syndrome 4 | |
| | | Single nucleotide variant (nonsense +1 more) | Bardet-Biedl syndrome 4 +1 more | GPathogenic/Likely pathogenic |
| | | Deletion (frameshift variant +1 more) | Bardet-Biedl syndrome 4 | |
| | | Single nucleotide variant (splice donor variant) | Bardet-Biedl syndrome +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Bardet-Biedl syndrome 4 | |
| | | Insertion (nonsense +1 more) | Bardet-Biedl syndrome 4 | |
| | | Single nucleotide variant (missense variant +1 more) | Bardet-Biedl syndrome 4 | |
Click to view in NCBI Gene