Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs267606745
rs267606745
A 0.800 CausalMutation CLINVAR

dbSNP: rs573527081
rs573527081
T 0.700 GeneticVariation CLINVAR Exome sequencing reveals novel variants and unique allelic spectrum for hearing impairment in Filipino cochlear implantees. 30828794

2019

dbSNP: rs1363680371
rs1363680371
CT 0.700 GeneticVariation CLINVAR The clinical spectrum of type IV collagen mutations. 9195222

1997

dbSNP: rs1057516204
rs1057516204
G 0.700 CausalMutation CLINVAR

dbSNP: rs1057519376
rs1057519376
C 0.700 CausalMutation CLINVAR

dbSNP: rs1057519377
rs1057519377
T 0.700 CausalMutation CLINVAR

dbSNP: rs1060499654
rs1060499654
T 0.700 CausalMutation CLINVAR

dbSNP: rs1175052474
rs1175052474
AGAG 0.700 GeneticVariation CLINVAR

dbSNP: rs121912824
rs121912824
T 0.700 CausalMutation CLINVAR

dbSNP: rs1346138010
rs1346138010
T 0.700 CausalMutation CLINVAR

dbSNP: rs1553760558
rs1553760558
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1559890352
rs1559890352
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1559909384
rs1559909384
A 0.700 CausalMutation CLINVAR

dbSNP: rs1559914770
rs1559914770
A 0.700 CausalMutation CLINVAR

dbSNP: rs200287952
rs200287952
A 0.700 CausalMutation CLINVAR

dbSNP: rs202147112
rs202147112
A 0.700 GeneticVariation CLINVAR

dbSNP: rs748901402
rs748901402
A 0.700 GeneticVariation CLINVAR

dbSNP: rs757341933
rs757341933
C 0.700 GeneticVariation CLINVAR

dbSNP: rs760462252
rs760462252
T 0.700 CausalMutation CLINVAR

dbSNP: rs760846085
rs760846085
C 0.700 CausalMutation CLINVAR

dbSNP: rs766900945
rs766900945
T 0.700 CausalMutation CLINVAR

dbSNP: rs772708743
rs772708743
A 0.700 CausalMutation CLINVAR

dbSNP: rs773515249
rs773515249
A 0.700 GeneticVariation CLINVAR

dbSNP: rs983885088
rs983885088
C 0.700 GeneticVariation CLINVAR