rs17112190
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs17112190(A;A) |
| Make rs17112190(A;G) |
| Make rs17112190(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 96880089 |
| Gene | LCOR |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17112190 |
| dbSNP (classic) | rs17112190 |
| ClinGen | rs17112190 |
| ebi | rs17112190 |
| HLI | rs17112190 |
| Exac | rs17112190 |
| Gnomad | rs17112190 |
| Varsome | rs17112190 |
| LitVar | rs17112190 |
| Map | rs17112190 |
| PheGenI | rs17112190 |
| Biobank | rs17112190 |
| 1000 genomes | rs17112190 |
| hgdp | rs17112190 |
| ensembl | rs17112190 |
| geneview | rs17112190 |
| scholar | rs17112190 |
| rs17112190 | |
| pharmgkb | rs17112190 |
| gwascentral | rs17112190 |
| openSNP | rs17112190 |
| 23andMe | rs17112190 |
| SNPshot | rs17112190 |
| SNPdbe | rs17112190 |
| MSV3d | rs17112190 |
| GWAS Ctlg | rs17112190 |
| GMAF | 0.118 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 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 | 9E-7 |
| Odds Ratio | 1.80 [1.42-2.27] |
