rs6800901
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;T) | multiple myeloma risk ? | |
| (T;T) | 1.1 | 1.3x multiple myeloma risk |
| Make rs6800901(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 121435346 |
| Gene | POLQ |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6800901 |
| dbSNP (classic) | rs6800901 |
| ClinGen | rs6800901 |
| ebi | rs6800901 |
| HLI | rs6800901 |
| Exac | rs6800901 |
| Gnomad | rs6800901 |
| Varsome | rs6800901 |
| LitVar | rs6800901 |
| Map | rs6800901 |
| PheGenI | rs6800901 |
| Biobank | rs6800901 |
| 1000 genomes | rs6800901 |
| hgdp | rs6800901 |
| ensembl | rs6800901 |
| geneview | rs6800901 |
| scholar | rs6800901 |
| rs6800901 | |
| pharmgkb | rs6800901 |
| gwascentral | rs6800901 |
| openSNP | rs6800901 |
| 23andMe | rs6800901 |
| SNPshot | rs6800901 |
| SNPdbe | rs6800901 |
| MSV3d | rs6800901 |
| GWAS Ctlg | rs6800901 |
| GMAF | 0.2084 |
| Max Magnitude | 1.1 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23502783 ]
|
| Trait | Multiple myeloma (IgH translocation) |
| Title | The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma. |
| Risk Allele | A |
| P-val | 2E-6 |
| Odds Ratio | 1.31 [1.17-1.47] |
