Rs11190870
From SNPedia
| Orientation | plus |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11190870 |
| PheGenI | rs11190870 |
| nextbio | rs11190870 |
| hapmap | rs11190870 |
| 1000 genomes | rs11190870 |
| hgdp | rs11190870 |
| ensembl | rs11190870 |
| gopubmed | rs11190870 |
| geneview | rs11190870 |
| scholar | rs11190870 |
| rs11190870 | |
| pharmgkb | rs11190870 |
| gwascentral | rs11190870 |
| openSNP | rs11190870 |
| 23andMe | rs11190870 |
| 23andMe all | rs11190870 |
| SNP Nexus | |
| SNPshot | rs11190870 |
| SNPdbe | rs11190870 |
| MSV3d | rs11190870 |
| Chromosome | 10 |
| Orientation | plus |
| GMAF | 0.4226 |
| Position | 102979207 |
| Reference | GRCh37 37.1/132 |
| Max Magnitude |
| Make rs11190870(C;C) |
| Make rs11190870(C;T) |
| Make rs11190870(T;T) |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
[PMID 21331621] Genetic variants in ultraconserved elements and risk of breast cancer in Chinese population
The T allele of this SNP is associated with an increased risk of scoliosis in adolescent Japanese girls. [1]
| GWAS snp | |
|---|---|
| PMID | [PMID 22019779] |
| Trait | |
| Title | A genome-wide association study identifies common variants near LBX1 associated with adolescent idiopathic scoliosis. |
| Risk Allele | |
| P-val | 1E-19 |
| Odds Ratio | 1.5600 None |
