rs2904880
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs2904880(C;G) |
| Make rs2904880(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 16 |
| Position | 28933075 |
| Gene | CD19 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2904880 |
| dbSNP (classic) | rs2904880 |
| ClinGen | rs2904880 |
| ebi | rs2904880 |
| HLI | rs2904880 |
| Exac | rs2904880 |
| Gnomad | rs2904880 |
| Varsome | rs2904880 |
| LitVar | rs2904880 |
| Map | rs2904880 |
| PheGenI | rs2904880 |
| Biobank | rs2904880 |
| 1000 genomes | rs2904880 |
| hgdp | rs2904880 |
| ensembl | rs2904880 |
| geneview | rs2904880 |
| scholar | rs2904880 |
| rs2904880 | |
| pharmgkb | rs2904880 |
| gwascentral | rs2904880 |
| openSNP | rs2904880 |
| 23andMe | rs2904880 |
| SNPshot | rs2904880 |
| SNPdbe | rs2904880 |
| MSV3d | rs2904880 |
| GWAS Ctlg | rs2904880 |
| GMAF | 0.1827 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 21961844] Association study of B-cell marker gene polymorphisms in European Caucasian patients with systemic sclerosis
[PMID 19001137
] Toward targeting B cell cancers with CD4+ CTLs: identification of a CD19-encoded minor histocompatibility antigen using a novel genome-wide analysis.
| ClinVar | |
|---|---|
| Risk | rs2904880(G;G) |
| Alt | rs2904880(G;G) |
| Reference | Rs2904880(C;C) |
| Significance | Non-pathogenic |
| Disease | Common Variable Immune Deficiency not specified |
| Variation | info |
| Gene | NPIPB8 CD19 |
| CLNDBN | Common Variable Immune Deficiency, Recessive not specified |
| Reversed | 0 |
| HGVS | NC_000016.9:g.28944396C>G |
| CLNSRC | |
| CLNACC | RCV000325903.1, RCV000455749.1, |
