Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1861494
rs1861494
Entrez Id: 3458;100885789
Gene Symbol: IFNG;IFNG-AS1
IFNG;IFNG-AS1
CUI: C0022104
Disease:
Irritable Bowel Syndrome
0.010 GeneticVariation BEFREE IFNG rs1861494 polymorphism is associated with IBD disease severity and functional changes in both IFNG methylation and protein secretion. 25171510 2014