| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (intron variant) | CARD11-related condition +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Severe combined immunodeficiency due to CARD11 deficiency +1 more | |
Click to view in NCBI Gene