rs16882214
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs16882214(C;C) |
| Make rs16882214(C;G) |
| Make rs16882214(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 19443704 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs16882214 |
| dbSNP (classic) | rs16882214 |
| ClinGen | rs16882214 |
| ebi | rs16882214 |
| HLI | rs16882214 |
| Exac | rs16882214 |
| Gnomad | rs16882214 |
| Varsome | rs16882214 |
| LitVar | rs16882214 |
| Map | rs16882214 |
| PheGenI | rs16882214 |
| Biobank | rs16882214 |
| 1000 genomes | rs16882214 |
| hgdp | rs16882214 |
| ensembl | rs16882214 |
| geneview | rs16882214 |
| scholar | rs16882214 |
| rs16882214 | |
| pharmgkb | rs16882214 |
| gwascentral | rs16882214 |
| openSNP | rs16882214 |
| 23andMe | rs16882214 |
| SNPshot | rs16882214 |
| SNPdbe | rs16882214 |
| MSV3d | rs16882214 |
| GWAS Ctlg | rs16882214 |
| GMAF | 0.1198 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23354978 ]
|
| Trait | Breast cancer |
| Title | Genetic variants associated with breast cancer risk for Ashkenazi Jewish women with strong family histories but no identifiable BRCA1/2 mutation. |
| Risk Allele | |
| P-val | 2E-6 |
| Odds Ratio | 1.43 [NR] |
