Rs1126605
From SNPedia
| Orientation | minus |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1126605 |
| PheGenI | rs1126605 |
| nextbio | rs1126605 |
| hapmap | rs1126605 |
| 1000 genomes | rs1126605 |
| hgdp | rs1126605 |
| ensembl | rs1126605 |
| gopubmed | rs1126605 |
| geneview | rs1126605 |
| scholar | rs1126605 |
| rs1126605 | |
| pharmgkb | rs1126605 |
| gwascentral | rs1126605 |
| openSNP | rs1126605 |
| 23andMe | rs1126605 |
| 23andMe all | rs1126605 |
| SNP Nexus | |
| SNPshot | rs1126605 |
| SNPdbe | rs1126605 |
| MSV3d | rs1126605 |
| Gene | C1R |
| Merged from | Rs3813729 |
| Chromosome | 12 |
| Orientation | minus |
| GMAF | 0.1749 |
| Position | 7242204 |
| Reference | GRCh37.p5 37.3/135 |
| Max Magnitude |
| Make rs1126605(A;A) |
| Make rs1126605(A;G) |
| Make rs1126605(G;G) |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
[PMID 22170086] Polymorphisms in complement system genes and risk of non-Hodgkin lymphoma.
| GET Evidence | |
|---|---|
| C1R-E184K | |
| aa_change | Glu184Lys |
| aa_change_short | E184K |
| impact | not reviewed |
| qualified_impact | Insufficiently evaluated not reviewed |
| overall_frequency | 0.101665 |
| summary | |
