rs1126605
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1126605(A;A) |
| Make rs1126605(A;G) |
| Make rs1126605(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 7089608 |
| Gene | C1R |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1126605 |
| dbSNP (classic) | rs1126605 |
| ClinGen | rs1126605 |
| ebi | rs1126605 |
| HLI | rs1126605 |
| Exac | rs1126605 |
| Gnomad | rs1126605 |
| Varsome | rs1126605 |
| LitVar | rs1126605 |
| Map | rs1126605 |
| PheGenI | rs1126605 |
| Biobank | rs1126605 |
| 1000 genomes | rs1126605 |
| hgdp | rs1126605 |
| ensembl | rs1126605 |
| geneview | rs1126605 |
| scholar | rs1126605 |
| rs1126605 | |
| pharmgkb | rs1126605 |
| gwascentral | rs1126605 |
| openSNP | rs1126605 |
| 23andMe | rs1126605 |
| SNPshot | rs1126605 |
| SNPdbe | rs1126605 |
| MSV3d | rs1126605 |
| GWAS Ctlg | rs1126605 |
| Merged from | Rs3813729 |
| GMAF | 0.1754 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 22170086
] Polymorphisms in complement system genes and risk of non-Hodgkin lymphoma.
