Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2234688
rs2234688
IFNG ; IFNG-AS1
CUI: C0025281
Disease: Meniere Disease
Meniere Disease 		0.010 GeneticVariation BEFREE We investigated the association between functional allelic variants of MIF (rs35688089), IFNG (rs2234688) and TNFA (rs1800629) in patients with MD. 23179933

2013