| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | Van der Woude syndrome 1 +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Orofacial cleft 6, susceptibility to +3 more | GPathogenic/Likely pathogenic |
Click to view in NCBI Gene