rs1314913
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1314913(C;C) |
| Make rs1314913(C;T) |
| Make rs1314913(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 14 |
| Position | 68232877 |
| Gene | RAD51B |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1314913 |
| dbSNP (classic) | rs1314913 |
| ClinGen | rs1314913 |
| ebi | rs1314913 |
| HLI | rs1314913 |
| Exac | rs1314913 |
| Gnomad | rs1314913 |
| Varsome | rs1314913 |
| LitVar | rs1314913 |
| Map | rs1314913 |
| PheGenI | rs1314913 |
| Biobank | rs1314913 |
| 1000 genomes | rs1314913 |
| hgdp | rs1314913 |
| ensembl | rs1314913 |
| geneview | rs1314913 |
| scholar | rs1314913 |
| rs1314913 | |
| pharmgkb | rs1314913 |
| gwascentral | rs1314913 |
| openSNP | rs1314913 |
| 23andMe | rs1314913 |
| SNPshot | rs1314913 |
| SNPdbe | rs1314913 |
| MSV3d | rs1314913 |
| GWAS Ctlg | rs1314913 |
| GMAF | 0.1084 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23001122 ]
|
| Trait | Breast cancer (male) |
| Title | Genome-wide association study identifies a common variant in RAD51B associated with male breast cancer risk. |
| Risk Allele | |
| P-val | 3E-13 |
| Odds Ratio | 1.57 [1.39-1.77] |
[PMID 17903304] Framingham Heart Study 100K project: genome-wide associations for cardiovascular disease outcomes.
[PMID 17903306] Genome-wide association study of electrocardiographic and heart rate variability traits: the Framingham Heart Study.
[PMID 26248686] Novel and known genetic variants for male breast cancer risk at 8q24.21, 9p21.3, 11q13.3 and 14q24.1: Results from a multicenter study in Italy
