Variant | Gene | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||
---|---|---|---|---|---|---|---|---|---|---|
|
T | 0.700 | GeneticVariation | GWASCAT | Sequence variants associating with urinary biomarkers. | 30476138 | 2019 |
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|
A | 0.700 | GeneticVariation | GWASCAT | Sequence variants associating with urinary biomarkers. | 30476138 | 2019 |
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|
G | 0.700 | SusceptibilityMutation | CLINVAR | Association of trypanolytic ApoL1 variants with kidney disease in African Americans. | 20647424 | 2010 |
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|
G | 0.700 | SusceptibilityMutation | CLINVAR | Association of trypanolytic ApoL1 variants with kidney disease in African Americans. | 20647424 | 2010 |
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|
A | 0.700 | CausalMutation | CLINVAR | NPHS2 (podicin) mutations in Turkish children with idiopathic nephrotic syndrome. | 17899208 | 2007 |
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|
A | 0.700 | CausalMutation | CLINVAR | A novel NPHS2 gene mutation in Turkish children with familial steroid-resistant nephrotic syndrome. | 15504144 | 2004 |
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|
A | 0.700 | CausalMutation | CLINVAR | Plasma membrane targeting of podocin through the classical exocytic pathway: effect of NPHS2 mutations. | 14675423 | 2004 |
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|
A | 0.700 | CausalMutation | CLINVAR | NPHS2 mutation analysis shows genetic heterogeneity of steroid-resistant nephrotic syndrome and low post-transplant recurrence. | 15253708 | 2004 |
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|
A | 0.700 | CausalMutation | CLINVAR | Patients with mutations in NPHS2 (podocin) do not respond to standard steroid treatment of nephrotic syndrome. | 14978175 | 2004 |
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|
T | 0.700 | CausalMutation | CLINVAR | ||||||
|
AGAG | 0.700 | CausalMutation | CLINVAR | ||||||
|
T | 0.700 | GeneticVariation | CLINVAR | ||||||
|
A | 0.700 | CausalMutation | CLINVAR | ||||||
|
T | 0.700 | CausalMutation | CLINVAR | ||||||
|
G | 0.700 | CausalMutation | CLINVAR | ||||||
|
CA | 0.700 | GeneticVariation | CLINVAR | ||||||
|
T | 0.700 | CausalMutation | CLINVAR | ||||||
|
A | 0.700 | GeneticVariation | CLINVAR | ||||||
|
C | 0.700 | GeneticVariation | CLINVAR | ||||||
|
A | 0.700 | GeneticVariation | CLINVAR | ||||||
|
T | 0.700 | GeneticVariation | CLINVAR | ||||||
|
G | 0.700 | GeneticVariation | CLINVAR | ||||||
|
CAATA | 0.700 | GeneticVariation | CLINVAR | ||||||
|
C | 0.700 | CausalMutation | CLINVAR |