Gene: SLC26A4 ×
Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057516953
rs1057516953
SLC26A4 ; SLC26A4-AS1
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1057517303
rs1057517303
SLC26A4
A 0.700 CausalMutation CLINVAR

dbSNP: rs1057518810
rs1057518810
SLC26A4 ; SLC26A4-AS1
C 0.700 GeneticVariation CLINVAR

dbSNP: rs111033220
rs111033220
SLC26A4
T 0.700 CausalMutation CLINVAR

dbSNP: rs111033305
rs111033305
SLC26A4
A 0.700 CausalMutation CLINVAR

dbSNP: rs111033312
rs111033312
SLC26A4
A 0.700 CausalMutation CLINVAR

dbSNP: rs111033313
rs111033313
SLC26A4
G 0.700 CausalMutation CLINVAR

dbSNP: rs111033318
rs111033318
SLC26A4
A 0.700 GeneticVariation CLINVAR

dbSNP: rs111033380
rs111033380
SLC26A4
T 0.700 CausalMutation CLINVAR

dbSNP: rs111033380
rs111033380
SLC26A4
A 0.700 GeneticVariation CLINVAR

dbSNP: rs121908362
rs121908362
SLC26A4
G 0.700 CausalMutation CLINVAR

dbSNP: rs121908363
rs121908363
SLC26A4
T 0.700 CausalMutation CLINVAR

dbSNP: rs121908364
rs121908364
SLC26A4
T 0.700 CausalMutation CLINVAR

dbSNP: rs1284633493
rs1284633493
SLC26A4
T 0.700 CausalMutation CLINVAR

dbSNP: rs1399914687
rs1399914687
SLC26A4
C 0.700 CausalMutation CLINVAR

dbSNP: rs147952620
rs147952620
SLC26A4
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1554352234
rs1554352234
SLC26A4 ; SLC26A4-AS1
G 0.700 CausalMutation CLINVAR

dbSNP: rs1554352676
rs1554352676
SLC26A4 ; SLC26A4-AS1
T 0.700 CausalMutation CLINVAR

dbSNP: rs1554355011
rs1554355011
SLC26A4
A 0.700 CausalMutation CLINVAR

dbSNP: rs1554360358
rs1554360358
SLC26A4
C 0.700 CausalMutation CLINVAR

dbSNP: rs1554360678
rs1554360678
SLC26A4
AT 0.700 CausalMutation CLINVAR

dbSNP: rs1554360816
rs1554360816
SLC26A4
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1554362735
rs1554362735
SLC26A4
AGCTGG 0.700 CausalMutation CLINVAR

dbSNP: rs1562835480
rs1562835480
SLC26A4
T 0.700 CausalMutation CLINVAR

dbSNP: rs1562835515
rs1562835515
SLC26A4
G 0.700 CausalMutation CLINVAR