Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs151344517
rs151344517
AFG3L2 ; TUBB6 ; LOC107985154
T 0.700 CausalMutation CLINVAR Missense mutations in the AFG3L2 proteolytic domain account for ∼1.5% of European autosomal dominant cerebellar ataxias. 20725928

2010
dbSNP: rs1178187217
rs1178187217
DNAH11
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1555735545
rs1555735545
STRN4 ; FKRP
A 0.700 CausalMutation CLINVAR

dbSNP: rs201943194
rs201943194
DNAH11
T 0.700 CausalMutation CLINVAR

dbSNP: rs267607261
rs267607261
MPV17
T 0.700 CausalMutation CLINVAR

dbSNP: rs28937900
rs28937900
FKRP
A 0.700 CausalMutation CLINVAR

dbSNP: rs368900406
rs368900406
MPV17
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1110149
rs1110149
GDNF ; GDNF-AS1
0.010 GeneticVariation BEFREE Heterozygosity was significantly lower for GDNF rs1110149 polymorphism in tinnitus subjects compared to the controls (p < 0.05). 27180191

2016
dbSNP: rs1800795
rs1800795
IL6 ; STEAP1B ; IL6-AS1
0.010 GeneticVariation BEFREE We found significant association between the genotype and allele frequencies of the IL6 -174 gene (rs1800795) and tinnitus among the elderly with history of exposure to occupational noise (P = 0.03). 26572700

2016
dbSNP: rs1805127
rs1805127
KCNE1
0.010 GeneticVariation BEFREE After adjustment, rs426496 was significantly associated with tinnitus during the initial crisis and with altered electronystagmography, and rs1805127 was significantly associated with nephropathy. 27509294

2016
dbSNP: rs3812047
rs3812047
GDNF ; GDNF-AS1
0.010 GeneticVariation BEFREE No correlation could be detected between GDNF rs884344 and rs3812047 polymorphisms and subjects with tinnitus (p > 0.05). 27180191

2016
dbSNP: rs426496
rs426496
AQP2 ; LOC101927318
0.010 GeneticVariation BEFREE The polymorphism rs426496, in AQP2, is associated with tinnitus at the onset of Ménière's disease and altered electronystagmography. 27509294

2016
dbSNP: rs884344
rs884344
GDNF ; GDNF-AS1
0.010 GeneticVariation BEFREE No correlation could be detected between GDNF rs884344 and rs3812047 polymorphisms and subjects with tinnitus (p > 0.05). 27180191

2016
dbSNP: rs12140311
rs12140311
CLCNKB
0.010 GeneticVariation BEFREE Tinnitus tended to be more frequent in ClC-Kb(T481S) carriers, a difference, however, not statistically significant. 16549283

2006