rs17293632
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs17293632(C;C) |
| Make rs17293632(C;T) |
| Make rs17293632(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 15 |
| Position | 67150258 |
| Gene | SMAD3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17293632 |
| dbSNP (classic) | rs17293632 |
| ClinGen | rs17293632 |
| ebi | rs17293632 |
| HLI | rs17293632 |
| Exac | rs17293632 |
| Gnomad | rs17293632 |
| Varsome | rs17293632 |
| LitVar | rs17293632 |
| Map | rs17293632 |
| PheGenI | rs17293632 |
| Biobank | rs17293632 |
| 1000 genomes | rs17293632 |
| hgdp | rs17293632 |
| ensembl | rs17293632 |
| geneview | rs17293632 |
| scholar | rs17293632 |
| rs17293632 | |
| pharmgkb | rs17293632 |
| gwascentral | rs17293632 |
| openSNP | rs17293632 |
| 23andMe | rs17293632 |
| SNPshot | rs17293632 |
| SNPdbe | rs17293632 |
| MSV3d | rs17293632 |
| GWAS Ctlg | rs17293632 |
| GMAF | 0.1079 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21102463 ]
|
| Trait | |
| Title | Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci |
| Risk Allele | T |
| P-val | 3E-19 |
| Odds Ratio | 1.1200 [1.07-1.16] |
| GWAS snp | |
|---|---|
| PMID | [PMID 23128233]
|
| Trait | Inflammatory bowel disease |
| Title | Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease. |
| Risk Allele | T |
| P-val | 6E-16 |
| Odds Ratio | 1.07 [1.032-1.102] |
[PMID 24121259] The Influence of CTGF Single-Nucleotide Polymorphisms on Outcomes in Crohn's Disease
