rs11171747
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs11171747(G;G) |
| Make rs11171747(G;T) |
| Make rs11171747(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 56124624 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11171747 |
| dbSNP (classic) | rs11171747 |
| ClinGen | rs11171747 |
| ebi | rs11171747 |
| HLI | rs11171747 |
| Exac | rs11171747 |
| Gnomad | rs11171747 |
| Varsome | rs11171747 |
| LitVar | rs11171747 |
| Map | rs11171747 |
| PheGenI | rs11171747 |
| Biobank | rs11171747 |
| 1000 genomes | rs11171747 |
| hgdp | rs11171747 |
| ensembl | rs11171747 |
| geneview | rs11171747 |
| scholar | rs11171747 |
| rs11171747 | |
| pharmgkb | rs11171747 |
| gwascentral | rs11171747 |
| openSNP | rs11171747 |
| 23andMe | rs11171747 |
| SNPshot | rs11171747 |
| SNPdbe | rs11171747 |
| MSV3d | rs11171747 |
| GWAS Ctlg | rs11171747 |
| GMAF | 0.3104 |
| Max Magnitude | 0 |
| ? | (G;G) (G;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 | 6E-8 |
| Odds Ratio | 1.2300 [1.14-1.33] |
[PMID 19956108] Analysis of 55 autoimmune disease and type II diabetes loci: further confirmation of chromosomes 4q27, 12q13.2 and 12q24.13 as type I diabetes loci, and support for a new locus, 12q13.3-q14.1.
