rs2055729
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2055729(A;A) |
| Make rs2055729(A;G) |
| Make rs2055729(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 8 |
| Position | 9935152 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2055729 |
| dbSNP (classic) | rs2055729 |
| ClinGen | rs2055729 |
| ebi | rs2055729 |
| HLI | rs2055729 |
| Exac | rs2055729 |
| Gnomad | rs2055729 |
| Varsome | rs2055729 |
| LitVar | rs2055729 |
| Map | rs2055729 |
| PheGenI | rs2055729 |
| Biobank | rs2055729 |
| 1000 genomes | rs2055729 |
| hgdp | rs2055729 |
| ensembl | rs2055729 |
| geneview | rs2055729 |
| scholar | rs2055729 |
| rs2055729 | |
| pharmgkb | rs2055729 |
| gwascentral | rs2055729 |
| openSNP | rs2055729 |
| 23andMe | rs2055729 |
| SNPshot | rs2055729 |
| SNPdbe | rs2055729 |
| MSV3d | rs2055729 |
| GWAS Ctlg | rs2055729 |
| GMAF | 0.489 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23502783 ]
|
| Trait | Multiple myeloma (hyperdiploidy) |
| Title | The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma. |
| Risk Allele | G |
| P-val | 8E-7 |
| Odds Ratio | 1.30 [1.17-1.45] |
