Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104894403
rs104894403
GJB2
A 0.710 GeneticVariation CLINVAR

dbSNP: rs1057517694
rs1057517694
CEP78
A 0.700 CausalMutation CLINVAR

dbSNP: rs1057517695
rs1057517695
CEP78
C 0.700 CausalMutation CLINVAR

dbSNP: rs1057518895
rs1057518895
AIFM1 ; RAB33A
G 0.700 GeneticVariation CLINVAR

dbSNP: rs111033437
rs111033437
MYO7A
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1302739538
rs1302739538
GJB2
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1348505504
rs1348505504
GIPC3
A 0.700 GeneticVariation CLINVAR

dbSNP: rs144948296
rs144948296
CKMT1B ; STRC
A 0.700 CausalMutation CLINVAR

dbSNP: rs1553212868
rs1553212868
POGZ
C 0.700 CausalMutation CLINVAR

dbSNP: rs1555661648
rs1555661648
AQP4 ; AQP4-AS1
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1555741826
rs1555741826
PRR12
G 0.700 CausalMutation CLINVAR

dbSNP: rs1558939623
rs1558939623
CHN1
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1559320299
rs1559320299
PAX3 ; CCDC140
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1564494285
rs1564494285
RET
C 0.700 CausalMutation CLINVAR

dbSNP: rs1566304640
rs1566304640
EDNRB ; EDNRB-AS1
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1567498374
rs1567498374
KARS1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1569167515
rs1569167515
POLR2F ; SOX10
G 0.700 CausalMutation CLINVAR

dbSNP: rs1569169328
rs1569169328
POLR2F ; SOX10
T 0.700 CausalMutation CLINVAR

dbSNP: rs1569492161
rs1569492161
COL4A5
C 0.700 CausalMutation CLINVAR

dbSNP: rs199474657
rs199474657
ND1 ; ND2 ; TRNL1
G 0.700 CausalMutation CLINVAR

dbSNP: rs200455852
rs200455852
ASAH1
G 0.700 CausalMutation CLINVAR

dbSNP: rs281874674
rs281874674
COL4A5
C 0.700 GeneticVariation CLINVAR

dbSNP: rs28931593
rs28931593
GJB2
T 0.700 CausalMutation CLINVAR

dbSNP: rs372466080
rs372466080
MYO15A
T 0.700 CausalMutation CLINVAR

dbSNP: rs397516875
rs397516875
GJB2
A 0.700 CausalMutation CLINVAR