Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121907896
rs121907896
SLC22A12
0.810 GeneticVariation UNIPROT

dbSNP: rs121907893
rs121907893
SLC22A12
T 0.800 CausalMutation CLINVAR

dbSNP: rs121907893
rs121907893
SLC22A12
0.800 GeneticVariation UNIPROT

dbSNP: rs121907894
rs121907894
SLC22A12
T 0.800 CausalMutation CLINVAR

dbSNP: rs121907894
rs121907894
SLC22A12
0.800 GeneticVariation UNIPROT

dbSNP: rs121907895
rs121907895
SLC22A12
G 0.800 CausalMutation CLINVAR

dbSNP: rs121907895
rs121907895
SLC22A12
0.800 GeneticVariation UNIPROT

dbSNP: rs121907897
rs121907897
SLC22A12
T 0.700 CausalMutation CLINVAR

dbSNP: rs149722479
rs149722479
SLC22A12
0.700 GeneticVariation UNIPROT

dbSNP: rs773677616
rs773677616
SLC22A12
0.700 GeneticVariation UNIPROT

dbSNP: rs765990518
rs765990518
SLC22A12
0.800 GeneticVariation UNIPROT Molecular identification of a renal urate anion exchanger that regulates blood urate levels. 12024214

2002
dbSNP: rs121907892
rs121907892
SLC22A12
A 0.750 CausalMutation CLINVAR Molecular identification of a renal urate anion exchanger that regulates blood urate levels. 12024214

2002
dbSNP: rs1047976958
rs1047976958
SLC22A12
0.700 GeneticVariation UNIPROT Molecular identification of a renal urate anion exchanger that regulates blood urate levels. 12024214

2002
dbSNP: rs201181059
rs201181059
SLC22A12
0.700 GeneticVariation UNIPROT Molecular identification of a renal urate anion exchanger that regulates blood urate levels. 12024214

2002
dbSNP: rs121907892
rs121907892
SLC22A12
A 0.750 CausalMutation CLINVAR Two male siblings with hereditary renal hypouricemia and exercise-induced ARF. 14655203

2003
dbSNP: rs121907896
rs121907896
SLC22A12
A 0.810 CausalMutation CLINVAR Clinical and molecular analysis of patients with renal hypouricemia in Japan-influence of URAT1 gene on urinary urate excretion. 14694169

2004
dbSNP: rs121907896
rs121907896
SLC22A12
A 0.810 CausalMutation CLINVAR A high prevalence of renal hypouricemia caused by inactive SLC22A12 in Japanese. 15327384

2004
dbSNP: rs765990518
rs765990518
SLC22A12
0.800 GeneticVariation UNIPROT A high prevalence of renal hypouricemia caused by inactive SLC22A12 in Japanese. 15327384

2004
dbSNP: rs765990518
rs765990518
SLC22A12
T 0.800 GeneticVariation CLINVAR Clinical and molecular analysis of patients with renal hypouricemia in Japan-influence of URAT1 gene on urinary urate excretion. 14694169

2004
dbSNP: rs765990518
rs765990518
SLC22A12
0.800 GeneticVariation UNIPROT Clinical and molecular analysis of patients with renal hypouricemia in Japan-influence of URAT1 gene on urinary urate excretion. 14694169

2004
dbSNP: rs121907892
rs121907892
SLC22A12
0.750 GeneticVariation BEFREE The present study demonstrates that homozygous W258X mutation is the predominant genetic cause of idiopathic renal hypouricemia in Japanese patients. 15054642

2004
dbSNP: rs121907892
rs121907892
SLC22A12
A 0.750 CausalMutation CLINVAR The present study demonstrates that homozygous W258X mutation is the predominant genetic cause of idiopathic renal hypouricemia in Japanese patients. 15054642

2004
dbSNP: rs1047976958
rs1047976958
SLC22A12
0.700 GeneticVariation UNIPROT Clinical and molecular analysis of patients with renal hypouricemia in Japan-influence of URAT1 gene on urinary urate excretion. 14694169

2004
dbSNP: rs1047976958
rs1047976958
SLC22A12
0.700 GeneticVariation UNIPROT A high prevalence of renal hypouricemia caused by inactive SLC22A12 in Japanese. 15327384

2004
dbSNP: rs201181059
rs201181059
SLC22A12
0.700 GeneticVariation UNIPROT A high prevalence of renal hypouricemia caused by inactive SLC22A12 in Japanese. 15327384

2004