rs16886165
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs16886165(G;G) |
| Make rs16886165(G;T) |
| Make rs16886165(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 56727256 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs16886165 |
| dbSNP (classic) | rs16886165 |
| ClinGen | rs16886165 |
| ebi | rs16886165 |
| HLI | rs16886165 |
| Exac | rs16886165 |
| Gnomad | rs16886165 |
| Varsome | rs16886165 |
| LitVar | rs16886165 |
| Map | rs16886165 |
| PheGenI | rs16886165 |
| Biobank | rs16886165 |
| 1000 genomes | rs16886165 |
| hgdp | rs16886165 |
| ensembl | rs16886165 |
| geneview | rs16886165 |
| scholar | rs16886165 |
| rs16886165 | |
| pharmgkb | rs16886165 |
| gwascentral | rs16886165 |
| openSNP | rs16886165 |
| 23andMe | rs16886165 |
| SNPshot | rs16886165 |
| SNPdbe | rs16886165 |
| MSV3d | rs16886165 |
| GWAS Ctlg | rs16886165 |
| GMAF | 0.2383 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 19330030 ]
|
| Trait | Breast cancer |
| Title | A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1) |
| Risk Allele | G |
| P-val | 5E-7 |
| Odds Ratio | |
[PMID 22452962] A genome-wide association study identifies a breast cancer risk variant in ERBB4 at 2q34: results from the Seoul Breast Cancer Study
[PMID 22965832] Association of common genetic variants with breast cancer risk and clinicopathological characteristics in a Chinese population.
