rs2315008
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2315008(G;G) |
| Make rs2315008(G;T) |
| Make rs2315008(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 20 |
| Position | 63712604 |
| Gene | ZGPAT |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2315008 |
| dbSNP (classic) | rs2315008 |
| ClinGen | rs2315008 |
| ebi | rs2315008 |
| HLI | rs2315008 |
| Exac | rs2315008 |
| Gnomad | rs2315008 |
| Varsome | rs2315008 |
| LitVar | rs2315008 |
| Map | rs2315008 |
| PheGenI | rs2315008 |
| Biobank | rs2315008 |
| 1000 genomes | rs2315008 |
| hgdp | rs2315008 |
| ensembl | rs2315008 |
| geneview | rs2315008 |
| scholar | rs2315008 |
| rs2315008 | |
| pharmgkb | rs2315008 |
| gwascentral | rs2315008 |
| openSNP | rs2315008 |
| 23andMe | rs2315008 |
| SNPshot | rs2315008 |
| SNPdbe | rs2315008 |
| MSV3d | rs2315008 |
| GWAS Ctlg | rs2315008 |
| GMAF | 0.3747 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS | |
|---|---|
| SNP | rs2315008 |
| PubMedID | [PMID 18758464 ]
|
| Condition | Inflammatory bowel disease |
| Gene | TNFRSF6B |
| Risk Allele | G |
| pValue | 9.00E-015 |
| OR | 1.36 |
| 95% CI | 1.05-1.76 |
[PMID 19623168] Investigation of reported associations between the 20q13 and 21q22 loci and pediatric-onset Crohn's disease in Canadian children.
