| | | Deletion | Hyper-IgM syndrome type 2 | |
| | | Deletion | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (missense variant +1 more) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (synonymous variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (synonymous variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (missense variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (missense variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (synonymous variant +1 more) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (missense variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (missense variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (synonymous variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (intron variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (intron variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (intron variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (synonymous variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (missense variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (missense variant) | Hyper-IgM syndrome type 2 | |
| | | Inversion (missense variant +1 more) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (missense variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (missense variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (splice donor variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (intron variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (missense variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (synonymous variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (missense variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (synonymous variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (synonymous variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (intron variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (missense variant +1 more) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (missense variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (nonsense +1 more) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (missense variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (intron variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (missense variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (nonsense) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (synonymous variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (missense variant) | Hyper-IgM syndrome type 2 | |
| | | Insertion (intron variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (missense variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (synonymous variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (nonsense) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (missense variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (intron variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (missense variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (missense variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (synonymous variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (stop lost) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (missense variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (missense variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (missense variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (missense variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (missense variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (synonymous variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (intron variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (missense variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (missense variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (missense variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (missense variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (intron variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (synonymous variant) | Hyper-IgM syndrome type 2 | |
| | | Microsatellite (intron variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (missense variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (synonymous variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (splice donor variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (missense variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (missense variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (missense variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (nonsense) | Hyper-IgM syndrome type 2 | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Hyper-IgM syndrome type 2 | |
| | | Deletion (intron variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (intron variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (synonymous variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (intron variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (intron variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (synonymous variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (intron variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (synonymous variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (intron variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (synonymous variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (synonymous variant) | Hyper-IgM syndrome type 2 | |
| | | Insertion (intron variant) | Hyper-IgM syndrome type 2 | |
| | | Duplication (intron variant) | Hyper-IgM syndrome type 2 | |
| | | Insertion (intron variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (intron variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (synonymous variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (missense variant) | Hyper-IgM syndrome type 2 | |
| | | Deletion (inframe_deletion) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (missense variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (missense variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (missense variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (missense variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (intron variant) | Hyper-IgM syndrome type 2 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (splice acceptor variant) | Hyper-IgM syndrome type 2 | |
| | | Indel (missense variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (intron variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (missense variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases +1 more | |
| | | Single nucleotide variant (nonsense +1 more) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (missense variant) | Hyper-IgM syndrome type 2 | |
| | | Single nucleotide variant (missense variant) | Hyper-IgM syndrome type 2 | |