rs10801047
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10801047(A;A) |
| Make rs10801047(A;T) |
| Make rs10801047(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 191590226 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10801047 |
| dbSNP (classic) | rs10801047 |
| ClinGen | rs10801047 |
| ebi | rs10801047 |
| HLI | rs10801047 |
| Exac | rs10801047 |
| Gnomad | rs10801047 |
| Varsome | rs10801047 |
| LitVar | rs10801047 |
| Map | rs10801047 |
| PheGenI | rs10801047 |
| Biobank | rs10801047 |
| 1000 genomes | rs10801047 |
| hgdp | rs10801047 |
| ensembl | rs10801047 |
| geneview | rs10801047 |
| scholar | rs10801047 |
| rs10801047 | |
| pharmgkb | rs10801047 |
| gwascentral | rs10801047 |
| openSNP | rs10801047 |
| 23andMe | rs10801047 |
| SNPshot | rs10801047 |
| SNPdbe | rs10801047 |
| MSV3d | rs10801047 |
| GWAS Ctlg | rs10801047 |
| GMAF | 0.1878 |
| Max Magnitude | 0 |
| ? | (A;A) (A;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS | |
|---|---|
| SNP | rs10801047 |
| PubMedID | [PMID 17554261 ]
|
| Condition | Crohn's disease |
| Gene | Intergenic |
| Risk Allele | |
| pValue | 3.00E-008 |
| OR | 1.47 |
| 95% CI | 1.22-1.76 |
[PMID 18853133] Gene variants influencing measures of inflammation or predisposing to autoimmune and inflammatory diseases are not associated with the risk of type 2 diabetes.
[PMID 19140132] Unbiased estimation of odds ratios: combining genomewide association scans with replication studies.
