rs3813729
From SNPedia
| Merged into | rs1126605 |
| Orientation | minus |
| Stabilized | minus |
| Make rs3813729(A;A) |
| Make rs3813729(A;G) |
| Make rs3813729(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 7089608 |
| Gene | C1R |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3813729 |
| dbSNP (classic) | rs3813729 |
| ClinGen | rs3813729 |
| ebi | rs3813729 |
| HLI | rs3813729 |
| Exac | rs3813729 |
| Gnomad | rs3813729 |
| Varsome | rs3813729 |
| LitVar | rs3813729 |
| Map | rs3813729 |
| PheGenI | rs3813729 |
| Biobank | rs3813729 |
| 1000 genomes | rs3813729 |
| hgdp | rs3813729 |
| ensembl | rs3813729 |
| geneview | rs3813729 |
| scholar | rs3813729 |
| rs3813729 | |
| pharmgkb | rs3813729 |
| gwascentral | rs3813729 |
| openSNP | rs3813729 |
| 23andMe | rs3813729 |
| SNPshot | rs3813729 |
| SNPdbe | rs3813729 |
| MSV3d | rs3813729 |
| GWAS Ctlg | rs3813729 |
| Status | Merged into rs1126605 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 22170086
] Polymorphisms in complement system genes and risk of non-Hodgkin lymphoma
