Rs1926657
From SNPedia
| Orientation | plus |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1926657 |
| PheGenI | rs1926657 |
| nextbio | rs1926657 |
| hapmap | rs1926657 |
| 1000 genomes | rs1926657 |
| hgdp | rs1926657 |
| ensembl | rs1926657 |
| gopubmed | rs1926657 |
| geneview | rs1926657 |
| scholar | rs1926657 |
| rs1926657 | |
| pharmgkb | rs1926657 |
| gwascentral | rs1926657 |
| openSNP | rs1926657 |
| 23andMe | rs1926657 |
| 23andMe all | rs1926657 |
| SNP Nexus | |
| SNPshot | rs1926657 |
| SNPdbe | rs1926657 |
| MSV3d | rs1926657 |
| Gene | ABCC4 |
| Chromosome | 13 |
| Orientation | plus |
| GMAF | 0.2573 |
| Position | 95874956 |
| Reference | GRCh37 37.1/131 |
| Max Magnitude |
| Make rs1926657(C;C) |
| Make rs1926657(C;T) |
| Make rs1926657(T;T) |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
| GWAS | |
|---|---|
| SNP | rs1926657 |
| PubMedID | [PMID 17903305] |
| Condition | Breast cancer |
| Gene | ABCC4 |
| Risk Allele | |
| pValue | 2.00E-006 |
| OR | NA |
| 95% CI | |
| GET Evidence | |
|---|---|
| rs1926657 | |
| aa_change | |
| aa_change_short | |
| impact | pathogenic |
| qualified_impact | Insufficiently evaluated pathogenic |
| overall_frequency | 0.765625 |
| summary | |
