rs3219018
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in complete genomics |
| Make rs3219018(C;C) |
| Make rs3219018(C;G) |
| Reference | GRCh37 37.1/131 |
| Chromosome | 1 |
| Position | 161662856 |
| Gene | FCGR2B |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3219018 |
| dbSNP (classic) | rs3219018 |
| ClinGen | rs3219018 |
| ebi | rs3219018 |
| HLI | rs3219018 |
| Exac | rs3219018 |
| Gnomad | rs3219018 |
| Varsome | rs3219018 |
| LitVar | rs3219018 |
| Map | rs3219018 |
| PheGenI | rs3219018 |
| Biobank | rs3219018 |
| 1000 genomes | rs3219018 |
| hgdp | rs3219018 |
| ensembl | rs3219018 |
| geneview | rs3219018 |
| scholar | rs3219018 |
| rs3219018 | |
| pharmgkb | rs3219018 |
| gwascentral | rs3219018 |
| openSNP | rs3219018 |
| 23andMe | rs3219018 |
| SNPshot | rs3219018 |
| SNPdbe | rs3219018 |
| MSV3d | rs3219018 |
| GWAS Ctlg | rs3219018 |
| Max Magnitude | 0 |
[PMID 15895258] Decreased transcription of the human FCGR2B gene mediated by the -343 G/C promoter polymorphism and association with systemic lupus erythematosus.
[PMID 18759263
] Features associated with, and the impact of, hemolytic anemia in patients with systemic lupus erythematosus: LX, results from a multiethnic cohort.
