Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1567396832
rs1567396832
OTOA
T 0.700 GeneticVariation CLINVAR Exome sequencing reveals novel variants and unique allelic spectrum for hearing impairment in Filipino cochlear implantees. 30828794

2019
dbSNP: rs1060499804
rs1060499804
OTOA
T 0.700 CausalMutation CLINVAR

dbSNP: rs1567381218
rs1567381218
OTOA
C 0.700 CausalMutation CLINVAR

dbSNP: rs200656442
rs200656442
OTOA
A 0.700 CausalMutation CLINVAR

dbSNP: rs587777133
rs587777133
OTOA
T 0.700 CausalMutation CLINVAR

dbSNP: rs751447996
rs751447996
OTOA
A 0.700 GeneticVariation CLINVAR

dbSNP: rs774366025
rs774366025
OTOA
G 0.700 GeneticVariation CLINVAR