rs2048672
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs2048672(G;G) |
| Make rs2048672(G;T) |
| Make rs2048672(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 130969092 |
| Gene | LINC-PINT |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2048672 |
| dbSNP (classic) | rs2048672 |
| ClinGen | rs2048672 |
| ebi | rs2048672 |
| HLI | rs2048672 |
| Exac | rs2048672 |
| Gnomad | rs2048672 |
| Varsome | rs2048672 |
| LitVar | rs2048672 |
| Map | rs2048672 |
| PheGenI | rs2048672 |
| Biobank | rs2048672 |
| 1000 genomes | rs2048672 |
| hgdp | rs2048672 |
| ensembl | rs2048672 |
| geneview | rs2048672 |
| scholar | rs2048672 |
| rs2048672 | |
| pharmgkb | rs2048672 |
| gwascentral | rs2048672 |
| openSNP | rs2048672 |
| 23andMe | rs2048672 |
| SNPshot | rs2048672 |
| SNPdbe | rs2048672 |
| MSV3d | rs2048672 |
| GWAS Ctlg | rs2048672 |
| GMAF | 0.4917 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21908515 ]
|
| Trait | |
| Title | Genome-wide association study identifies breast cancer risk variant at 10q21.2: results from the Asia Breast Cancer Consortium. |
| Risk Allele | C |
| P-val | 0.000006 |
| Odds Ratio | 1.1100 [1.05-1.17] |
[PMID 24127041] Polymorphisms in ESR1 and FLJ43663 are associated with breast cancer risk in the Han population
