Gene: EPHX2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2053
Gene Symbol: EPHX2
EPHX2 		0.610 GeneticVariation disease BEFREE These results indicate a significant modification of the phenotype of FH with defective LDLR allele by EPHX2-287Arg variation in our studied kindred. 14673705 2004
Entrez Id: 2053
Gene Symbol: EPHX2
EPHX2 		0.610 SusceptibilityMutation disease CLINVAR
Entrez Id: 2053
Gene Symbol: EPHX2
EPHX2 		0.610 Biomarker disease CTD_human
Entrez Id: 2053
Gene Symbol: EPHX2
EPHX2 		0.610 Biomarker disease GENOMICS_ENGLAND