Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs181509591
rs181509591
SLC2A9 ; LOC105374476
0.800 GeneticVariation UNIPROT Two novel homozygous SLC2A9 mutations cause renal hypouricemia type 2. 21810765

2012
dbSNP: rs181509591
rs181509591
SLC2A9 ; LOC105374476
0.800 GeneticVariation UNIPROT Homozygous SLC2A9 mutations cause severe renal hypouricemia. 19926891

2010
dbSNP: rs181509591
rs181509591
SLC2A9 ; LOC105374476
0.800 GeneticVariation UNIPROT Mutations in glucose transporter 9 gene SLC2A9 cause renal hypouricemia. 19026395

2008
dbSNP: rs181509591
rs181509591
SLC2A9 ; LOC105374476
A 0.800 CausalMutation CLINVAR