rs11047102
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs11047102(C;C) |
| Make rs11047102(C;T) |
| Make rs11047102(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 23793212 |
| Gene | SOX5 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11047102 |
| dbSNP (classic) | rs11047102 |
| ClinGen | rs11047102 |
| ebi | rs11047102 |
| HLI | rs11047102 |
| Exac | rs11047102 |
| Gnomad | rs11047102 |
| Varsome | rs11047102 |
| LitVar | rs11047102 |
| Map | rs11047102 |
| PheGenI | rs11047102 |
| Biobank | rs11047102 |
| 1000 genomes | rs11047102 |
| hgdp | rs11047102 |
| ensembl | rs11047102 |
| geneview | rs11047102 |
| scholar | rs11047102 |
| rs11047102 | |
| pharmgkb | rs11047102 |
| gwascentral | rs11047102 |
| openSNP | rs11047102 |
| 23andMe | rs11047102 |
| SNPshot | rs11047102 |
| SNPdbe | rs11047102 |
| MSV3d | rs11047102 |
| GWAS Ctlg | rs11047102 |
| GMAF | 0.0753 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21779181 ]
|
| Trait | |
| Title | Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy. |
| Risk Allele | |
| P-val | 1E-7 |
| Odds Ratio | 1.3600 [1.21-1.52] |
rs11047102 is associated with systemic sclerosis. [PMID 21779181]
