SLC2A9, solute carrier family 2 member 9, 56606

N. diseases: 74; N. variants: 389
Disease: Kidney Calculi ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1014290
rs1014290
Entrez Id: 56606;105374476
Gene Symbol: SLC2A9;LOC105374476
SLC2A9;LOC105374476
CUI: C0022650
Disease:
Kidney Calculi 		0.010 GeneticVariation BEFREE There was a weak but significant association of all 4 SNPs and nephrolithiasis (P=0.029 for rs733175; P=0.006 for rs6449213; P=0.020 for rs1014290, and P=0.011 for rs737267). 20162745 2010
dbSNP: rs6449213
rs6449213
Entrez Id: 56606;105374476
Gene Symbol: SLC2A9;LOC105374476
SLC2A9;LOC105374476
CUI: C0022650
Disease:
Kidney Calculi 		0.010 GeneticVariation BEFREE Logistic regression in an age- and sex-adjusted model suggested that genotype C/T for rs6449213 had odds ratio for nephrolithiasis of 2.89 (95% confidence interval 1.13-7.40). 20162745 2010
dbSNP: rs733175
rs733175
Entrez Id: 56606
Gene Symbol: SLC2A9
SLC2A9
CUI: C0022650
Disease:
Kidney Calculi 		0.010 GeneticVariation BEFREE There was a weak but significant association of all 4 SNPs and nephrolithiasis (P=0.029 for rs733175; P=0.006 for rs6449213; P=0.020 for rs1014290, and P=0.011 for rs737267). 20162745 2010
dbSNP: rs737267
rs737267
Entrez Id: 56606
Gene Symbol: SLC2A9
SLC2A9
CUI: C0022650
Disease:
Kidney Calculi 		0.010 GeneticVariation BEFREE There was a weak but significant association of all 4 SNPs and nephrolithiasis (P=0.029 for rs733175; P=0.006 for rs6449213; P=0.020 for rs1014290, and P=0.011 for rs737267). 20162745 2010