rs3096299
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs3096299(C;C) |
| Make rs3096299(C;T) |
| Make rs3096299(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 16 |
| Position | 89382255 |
| Gene | ANKRD11 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3096299 |
| dbSNP (classic) | rs3096299 |
| ClinGen | rs3096299 |
| ebi | rs3096299 |
| HLI | rs3096299 |
| Exac | rs3096299 |
| Gnomad | rs3096299 |
| Varsome | rs3096299 |
| LitVar | rs3096299 |
| Map | rs3096299 |
| PheGenI | rs3096299 |
| Biobank | rs3096299 |
| 1000 genomes | rs3096299 |
| hgdp | rs3096299 |
| ensembl | rs3096299 |
| geneview | rs3096299 |
| scholar | rs3096299 |
| rs3096299 | |
| pharmgkb | rs3096299 |
| gwascentral | rs3096299 |
| openSNP | rs3096299 |
| 23andMe | rs3096299 |
| SNPshot | rs3096299 |
| SNPdbe | rs3096299 |
| MSV3d | rs3096299 |
| GWAS Ctlg | rs3096299 |
| GMAF | 0.4467 |
| Max Magnitude | 0 |
| ? | (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 | G |
| P-val | 4E-6 |
| Odds Ratio | 1.54 [1.28-1.86] |
