Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2075252
rs2075252
T 0.700 GeneticVariation GWASCAT Sequence variants associating with urinary biomarkers. 30476138

2019

dbSNP: rs74375025
rs74375025
A 0.700 GeneticVariation GWASCAT Sequence variants associating with urinary biomarkers. 30476138

2019

dbSNP: rs1428826948
rs1428826948
G 0.700 SusceptibilityMutation CLINVAR Association of trypanolytic ApoL1 variants with kidney disease in African Americans. 20647424

2010

dbSNP: rs1569534160
rs1569534160
G 0.700 SusceptibilityMutation CLINVAR Association of trypanolytic ApoL1 variants with kidney disease in African Americans. 20647424

2010

dbSNP: rs869025495
rs869025495
A 0.700 CausalMutation CLINVAR NPHS2 (podicin) mutations in Turkish children with idiopathic nephrotic syndrome. 17899208

2007

dbSNP: rs869025495
rs869025495
A 0.700 CausalMutation CLINVAR Plasma membrane targeting of podocin through the classical exocytic pathway: effect of NPHS2 mutations. 14675423

2004

dbSNP: rs869025495
rs869025495
A 0.700 CausalMutation CLINVAR A novel NPHS2 gene mutation in Turkish children with familial steroid-resistant nephrotic syndrome. 15504144

2004

dbSNP: rs869025495
rs869025495
A 0.700 CausalMutation CLINVAR Patients with mutations in NPHS2 (podocin) do not respond to standard steroid treatment of nephrotic syndrome. 14978175

2004

dbSNP: rs869025495
rs869025495
A 0.700 CausalMutation CLINVAR NPHS2 mutation analysis shows genetic heterogeneity of steroid-resistant nephrotic syndrome and low post-transplant recurrence. 15253708

2004

dbSNP: rs1131692245
rs1131692245
T 0.700 CausalMutation CLINVAR

dbSNP: rs1175052474
rs1175052474
AGAG 0.700 CausalMutation CLINVAR

dbSNP: rs1272948499
rs1272948499
T 0.700 GeneticVariation CLINVAR

dbSNP: rs138924661
rs138924661
A 0.700 CausalMutation CLINVAR

dbSNP: rs1556411578
rs1556411578
T 0.700 CausalMutation CLINVAR

dbSNP: rs1556445736
rs1556445736
G 0.700 CausalMutation CLINVAR

dbSNP: rs1556463583
rs1556463583
CA 0.700 GeneticVariation CLINVAR

dbSNP: rs199840952
rs199840952
T 0.700 CausalMutation CLINVAR

dbSNP: rs267602852
rs267602852
WT1
A 0.700 GeneticVariation CLINVAR

dbSNP: rs281874674
rs281874674
C 0.700 GeneticVariation CLINVAR

dbSNP: rs530391015
rs530391015
A 0.700 GeneticVariation CLINVAR

dbSNP: rs533297350
rs533297350
T 0.700 GeneticVariation CLINVAR

dbSNP: rs569681869
rs569681869
G 0.700 GeneticVariation CLINVAR

dbSNP: rs779593707
rs779593707
CAATA 0.700 GeneticVariation CLINVAR

dbSNP: rs869025224
rs869025224
C 0.700 CausalMutation CLINVAR