| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | Epilepsy +6 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | WDR37-related condition +7 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Developmental delay +5 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +7 more | GPathogenic/Likely pathogenic |
Click to view in NCBI Gene