Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3732378
rs3732378
Entrez Id: 1524
Gene Symbol: CX3CR1
CX3CR1
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