SNX20, sorting nexin 20, 124460

N. diseases: 4; N. variants: 3
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.110 GeneticVariation disease BEFREE In addition, 9 genes previously associated with IBD contained SNPs with significant evidence for replication (P < 1.6 × 10<sup>-6</sup>): ADCY3, CXCR6, HLA-DRB1 to HLA-DQA1 (genome-wide significance on conditioning), IL12B,PTGER4, and TNC for IBD; IL23R, PTGER4, and SNX20 (in strong linkage disequilibrium with NOD2) for CD; and KCNQ2 (near TNFRSF6B) for UC. 27693347 2017
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.110 GeneticVariation disease GWASCAT Genetic architecture differences between pediatric and adult-onset inflammatory bowel diseases in the Polish population. 28008999 2016
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.110 GeneticVariation disease GWASDB Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci. 17804789 2007