| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (intron variant) | CTLA4-related disorder +1 more | |
| | | Single nucleotide variant (synonymous variant) | CTLA4-related disorder +1 more | |
| | | Single nucleotide variant (splice donor variant) | CTLA4-related disorder | |
| | | Single nucleotide variant (synonymous variant +1 more) | CTLA4-related disorder | |
| | | Single nucleotide variant (missense variant +1 more) | CTLA4-related disorder | |
Click to view in NCBI Gene