rs3732378, CX3CR1

N. diseases: 48
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Stenosis of intestine
CUI: C0267465
Disease: Stenosis of intestine
0.010 GeneticVariation BEFREE All T280M homozygotes were diagnosed of intestinal stenosis (p = 0.03 vs wildtype and heterozygous carriers) and had significantly more often ileocolonic involvement more often than patients with wildtype and heterozygous genotypes (p = 0.01). 16405540 2006