Rs1154865
From SNPedia
| Orientation | plus |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1154865 |
| PheGenI | rs1154865 |
| nextbio | rs1154865 |
| hapmap | rs1154865 |
| 1000 genomes | rs1154865 |
| hgdp | rs1154865 |
| ensembl | rs1154865 |
| gopubmed | rs1154865 |
| geneview | rs1154865 |
| scholar | rs1154865 |
| rs1154865 | |
| pharmgkb | rs1154865 |
| gwascentral | rs1154865 |
| openSNP | rs1154865 |
| 23andMe | rs1154865 |
| 23andMe all | rs1154865 |
| SNP Nexus | |
| SNPshot | rs1154865 |
| SNPdbe | rs1154865 |
| MSV3d | rs1154865 |
| Chromosome | 12 |
| Orientation | plus |
| GMAF | 0.2033 |
| Position | 73989837 |
| Reference | GRCh37 37.1/131 |
| Max Magnitude |
| Make rs1154865(C;C) |
| Make rs1154865(C;G) |
| Make rs1154865(G;G) |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
| GWAS | |
|---|---|
| SNP | rs1154865 |
| PubMedID | [PMID 17903305] |
| Condition | Breast cancer |
| Gene | Intergenic |
| Risk Allele | |
| pValue | 7.00E-007 |
| OR | NA |
| 95% CI | |
| GET Evidence | |
|---|---|
| rs1154865 | |
| aa_change | |
| aa_change_short | |
| impact | pathogenic |
| qualified_impact | Insufficiently evaluated pathogenic |
| overall_frequency | 0.203125 |
| summary | |
