Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4524
Gene Symbol: MTHFR
MTHFR 		0.300 Biomarker phenotype CTD_human Methylenetetrahydrofolate reductase gene mutations as risk factors for sudden hearing loss. 16275406 2006
Entrez Id: 1463
Gene Symbol: NCAN
NCAN 		0.010 AlteredExpression phenotype BEFREE The ECM variously participates in adaptive responses to sudden deafness by SD on several levels along the central auditory pathway, with a striking spatial and temporal relationship of Ncan modulation to astrocytic activation and to synaptogenesis. 31271523 2019
Entrez Id: 2706
Gene Symbol: GJB2
GJB2 		0.010 GeneticVariation phenotype BEFREE We sought to explore the frequency of GJB2 and mitochondrial 12S rRNA susceptibility mutations in patients with sudden deafness. 26119842 2016
Entrez Id: 4312
Gene Symbol: MMP1
MMP1 		0.010 GeneticVariation phenotype BEFREE At MMP1 -519A/G, there was no statistically significant increase in the risk of SD. 21154774 2011
Entrez Id: 3565
Gene Symbol: IL4
IL4 		0.010 GeneticVariation phenotype BEFREE IL4 receptor polymorphism is associated with increased risk of sudden deafness in Korean population. 16280132 2006
Entrez Id: 3566
Gene Symbol: IL4R
IL4R 		0.010 GeneticVariation phenotype BEFREE In this study we investigated the possible relationship between sudden deafness (SD) and IL4R polymorphism Q576R in 97 Korean SD patients and 613 controls using pyrosequencing method. 16280132 2006