| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | IRF2BP2, LOC129932811 (P238T) | Single nucleotide variant (missense variant) | IRF2BP2-related disorder +1 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | IRF2BP2-related disorder +1 more | |
Click to view in NCBI Gene