Gene: SLC26A2 ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104893920
rs104893920
SLC26A2
G 0.710 CausalMutation CLINVAR

dbSNP: rs121908078
rs121908078
SLC26A2
A 0.710 CausalMutation CLINVAR

dbSNP: rs104893916
rs104893916
SLC26A2
T 0.700 CausalMutation CLINVAR

dbSNP: rs104893921
rs104893921
SLC26A2
C 0.700 CausalMutation CLINVAR

dbSNP: rs1057517462
rs1057517462
SLC26A2
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1057517471
rs1057517471
SLC26A2
GT 0.700 GeneticVariation CLINVAR

dbSNP: rs1057517474
rs1057517474
SLC26A2
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1057517482
rs1057517482
SLC26A2
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1057517483
rs1057517483
SLC26A2
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1057517495
rs1057517495
SLC26A2
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1057517496
rs1057517496
SLC26A2
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1057517502
rs1057517502
SLC26A2
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1057517504
rs1057517504
SLC26A2
CCAGTG 0.700 GeneticVariation CLINVAR

dbSNP: rs1057517511
rs1057517511
SLC26A2
AGTTAT 0.700 GeneticVariation CLINVAR

dbSNP: rs1057517514
rs1057517514
SLC26A2
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1057517523
rs1057517523
SLC26A2
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1057517524
rs1057517524
SLC26A2
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1057517526
rs1057517526
SLC26A2
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1057517530
rs1057517530
SLC26A2
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1057517532
rs1057517532
SLC26A2
T 0.700 GeneticVariation CLINVAR

dbSNP: rs121908077
rs121908077
SLC26A2
C 0.700 CausalMutation CLINVAR

dbSNP: rs200963884
rs200963884
SLC26A2
C 0.700 GeneticVariation CLINVAR

dbSNP: rs267607055
rs267607055
SLC26A2
T 0.700 CausalMutation CLINVAR

dbSNP: rs386833492
rs386833492
SLC26A2
C 0.700 CausalMutation CLINVAR

dbSNP: rs386833493
rs386833493
SLC26A2
T 0.700 GeneticVariation CLINVAR