rs1078806
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1078806(C;C) |
| Make rs1078806(C;T) |
| Make rs1078806(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 121579461 |
| Gene | FGFR2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1078806 |
| dbSNP (classic) | rs1078806 |
| ClinGen | rs1078806 |
| ebi | rs1078806 |
| HLI | rs1078806 |
| Exac | rs1078806 |
| Gnomad | rs1078806 |
| Varsome | rs1078806 |
| LitVar | rs1078806 |
| Map | rs1078806 |
| PheGenI | rs1078806 |
| Biobank | rs1078806 |
| 1000 genomes | rs1078806 |
| hgdp | rs1078806 |
| ensembl | rs1078806 |
| geneview | rs1078806 |
| scholar | rs1078806 |
| rs1078806 | |
| pharmgkb | rs1078806 |
| gwascentral | rs1078806 |
| openSNP | rs1078806 |
| 23andMe | rs1078806 |
| SNPshot | rs1078806 |
| SNPdbe | rs1078806 |
| MSV3d | rs1078806 |
| GWAS Ctlg | rs1078806 |
| GMAF | 0.3343 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 21382839
] Relation of FGFR2 Genetic Polymorphisms to the Association Between Oral Contraceptive Use and the Risk of Breast Cancer in Chinese Women
[PMID 18326623] Genome-wide association study provides evidence for a breast cancer risk locus at 6q22.33.
[PMID 19738052] A risk variant in an miR-125b binding site in BMPR1B is associated with breast cancer pathogenesis.
| 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 | C |
| P-val | 2E-6 |
| Odds Ratio | 1.43 [NR] |
