Rs2315008
From SNPedia
| Orientation | plus |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2315008 |
| PheGenI | rs2315008 |
| nextbio | rs2315008 |
| hapmap | rs2315008 |
| 1000 genomes | rs2315008 |
| hgdp | rs2315008 |
| ensembl | rs2315008 |
| gopubmed | rs2315008 |
| geneview | rs2315008 |
| scholar | rs2315008 |
| rs2315008 | |
| pharmgkb | rs2315008 |
| gwascentral | rs2315008 |
| openSNP | rs2315008 |
| 23andMe | rs2315008 |
| 23andMe all | rs2315008 |
| SNP Nexus | |
| SNPshot | rs2315008 |
| SNPdbe | rs2315008 |
| MSV3d | rs2315008 |
| Gene | ZGPAT |
| Chromosome | 20 |
| Orientation | plus |
| GMAF | 0.375 |
| Position | 62343956 |
| Reference | GRCh37 37.1/131 |
| Max Magnitude |
| Make rs2315008(G;G) |
| Make rs2315008(G;T) |
| Make rs2315008(T;T) |
| ? | (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.
| GET Evidence | |
|---|---|
| rs2315008 | |
| aa_change | |
| aa_change_short | |
| impact | pathogenic |
| qualified_impact | Insufficiently evaluated pathogenic |
| overall_frequency | 0.773438 |
| summary | |
