Common Variable Immune Deficiency Explore Disorder's Alias
An Autosomal dominant, Autosomal recessive mode(s) within the Immune disorders category
Candidate Gene Information
An Autosomal dominant, Autosomal recessive mode(s) within the Immune disorders category
Reported Pathogenic variants
| S.No. | Name/GeneID | Description | Cytogentic Band | Gene Location on genomic DNA | Gene Length | Exons | Details | Gene Cross-References |
| 1 | CD19/930 | CD19 molecule | 16p11.2 | Chr16, NC_000016.10 (28931971..28939342) |
7372 nt | 14 | More... | OMIM gene gnomAD browser EnsEMBL GeneCards ClinGen gene |
| 2 | TNFRSF13B/23495 | TNF receptor superfamily member 13B | 17p11.2 | Chr17, NC_000017.11 (16939081..16972118, complement) |
33038 nt | 5 | More... | OMIM gene gnomAD browser EnsEMBL GeneCards ClinGen gene |
| 3 | TNFRSF13C/115650 | TNF receptor superfamily member 13C | 22q13.2 | Chr22, NC_000022.11 (41922032..41926806, complement) |
4775 nt | 3 | More... | OMIM gene gnomAD browser EnsEMBL GeneCards ClinGen gene |
| Variant Information | ||||||||
| Disorder Cross-References: GARD GTR MalaCards NORD | ||||||||
Patient care services
Clinical Symptoms & Disabilities
Prevalence
| Under development |