rs12659144
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs12659144(C;C) |
| Make rs12659144(C;T) |
| Make rs12659144(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 174350517 |
| Gene | LINC01411 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs12659144 |
| dbSNP (classic) | rs12659144 |
| ClinGen | rs12659144 |
| ebi | rs12659144 |
| HLI | rs12659144 |
| Exac | rs12659144 |
| Gnomad | rs12659144 |
| Varsome | rs12659144 |
| LitVar | rs12659144 |
| Map | rs12659144 |
| PheGenI | rs12659144 |
| Biobank | rs12659144 |
| 1000 genomes | rs12659144 |
| hgdp | rs12659144 |
| ensembl | rs12659144 |
| geneview | rs12659144 |
| scholar | rs12659144 |
| rs12659144 | |
| pharmgkb | rs12659144 |
| gwascentral | rs12659144 |
| openSNP | rs12659144 |
| 23andMe | rs12659144 |
| SNPshot | rs12659144 |
| SNPdbe | rs12659144 |
| MSV3d | rs12659144 |
| GWAS Ctlg | rs12659144 |
| GMAF | 0.2236 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 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 | 3E-6 |
| Odds Ratio | 1.67 [1.35-2.07] |
