rs17466684, EPHX2

N. diseases: 5
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Panic Disorder
CUI: C0030319
Disease: Panic Disorder
0.800 GeneticVariation GWASDB Genome-wide association study of panic disorder in the Japanese population. 19165232 2009
Panic Disorder
CUI: C0030319
Disease: Panic Disorder
0.800 GeneticVariation GWASCAT Genome-wide association study of panic disorder in the Japanese population. 19165232 2009
Gestational Diabetes
CUI: C0085207
Disease: Gestational Diabetes
0.010 GeneticVariation BEFREE The SNP of <i>EPHX2</i> (rs17466684) gene polymorphism is associated with depression symptoms among Malaysian women with GDM. 31801286 2019
Depressive Symptoms
CUI: C0086132
Disease: Depressive Symptoms
0.010 GeneticVariation BEFREE The SNP of <i>EPHX2</i> (rs17466684) gene polymorphism is associated with depression symptoms among Malaysian women with GDM. 31801286 2019
Symptoms of stress
CUI: C0521991
Disease: Symptoms of stress
0.010 GeneticVariation BEFREE SNP of <i>EPHX2</i> (rs17466684), <i>OXTR</i> (rs53576) and <i>NRG1</i> (rs2919375) are also associated with stress symptoms. 31801286 2019
Fish-Eye Disease
CUI: C0342895
Disease: Fish-Eye Disease
0.010 GeneticVariation BEFREE SNP analysis identified an association of TCF4 (rs613872 (P=5.25 × 10(-15), OR=4.05), rs9954153 (P=3.37 × 10(-7), OR=2.58), rs2286812 (P=4.23 × 10(-6), OR=2.55) and rs17595731 (P=3.57 × 10(-5), OR=3.79)), CLU (rs17466684; P=0.003, OR=1.85) and one haplotype of TGFBI SNPs (P=0.011, OR=2.29) with FED in Caucasian Australians. 22234156 2012