rs13361189, None

N. diseases: 13
Disease: Ileal Diseases ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Ileal Diseases
CUI: C0020875
Disease: Ileal Diseases
0.010 GeneticVariation BEFREE The SNP rs13361189 was also found to increase the risk of Crohn's disease clinical sub-phenotype (fibrostricturing behaviour, ileal disease, perianal disease, intestinal resection). 26066377 2015