| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (3 prime UTR variant) | Hyper-IgM syndrome type 2 +2 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +2 more | |
| | | Duplication (intron variant) | not provided +3 more | |
| | | Single nucleotide variant (intron variant) | not specified +2 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Hyper-IgM syndrome type 2 +3 more | |
Click to view in NCBI Gene