Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1131692231
rs1131692231
CYFIP2
T 0.700 CausalMutation CLINVAR

dbSNP: rs199469465
rs199469465
SRCAP
T 0.700 CausalMutation CLINVAR

dbSNP: rs770861172
rs770861172
DNAH7
T 0.700 CausalMutation CLINVAR

dbSNP: rs5743708
rs5743708
TLR2
0.010 GeneticVariation BEFREE Significant association between TLR 2 Arg753Gln polymorphism and different types of mucosal changes in patients with chronic otitis media was established. 26055429

2015
dbSNP: rs121913657
rs121913657
MYH9
0.010 GeneticVariation BEFREE Our patient was a 13-year-old girl with an MYH9 S96L missense mutation who required a tympanoplasty due to chronic otitis media. 23940247

2013
dbSNP: rs4986790
rs4986790
TLR4
0.010 GeneticVariation BEFREE In this study, the effect of the molecular reasons which display genetic differences in TS formation is evaluated; our aim is to determine the Asp299Gly polymorphism frequencies in the TLR4 gene of patients with TS who have COM, and patients who do not. 19398177

2010