| GWAS snp
|
| PMID
|
[PMID 18587394 ]
|
| Trait
|
Crohn's disease
|
| Title
|
Genome-wide assocation defines more than 30 distinct susceptibility loci for Crohn's disease
|
| Risk Allele
|
G
|
| P-val
|
3E-10
|
| Odds Ratio
|
1.22 [NR]
|
| OMIM | 612259 |
| Desc | INFLAMMATORY BOWEL DISEASE 16; IBD16 |
| Variant | |
| Related | also |
[PMID 21636646] Association of TNFSF15 polymorphism with irritable bowel syndrome
[PMID 19557189] Identifying relationships among genomic disease regions: predicting genes at pathogenic SNP associations and rare deletions.
[PMID 21304977] An investigation of genome-wide studies reported susceptibility loci for ulcerative colitis shows limited replication in north Indians.
[PMID 25028192] Associations between TNFSF15 polymorphisms and susceptibility to ulcerative colitis and Crohn's disease: A meta-analysis
[PMID 25824902] A meta-analysis of immunogenetic Case-Control Association Studies in irritable bowel syndrome
[PMID 25501099] Protective association of tumor necrosis factor superfamily 15 (TNFSF15) polymorphic haplotype with Ulcerative Colitis and Crohn's disease in an Indian population
[PMID 27647972] A case-control study about the association between vascular endothelial growth inhibitor gene polymorphisms and breast cancer risk in female patients in Northeast China.
[PMID 29446656] Crohn's Disease Candidate Gene Alleles Predict Time to Progression from Inflammatory B1 to Stricturing B2, or Penetrating B3 Phenotype.
[PMID 31615448] Candidate single nucleotide polymorphisms of irritable bowel syndrome: a systemic review and meta-analysis.
]
