| Variant | Gene | Disease | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
|
0.800 | GeneticVariation | UNIPROT | ||||||||||
|
|
|
0.700 | GeneticVariation | UNIPROT | ||||||||||
|
|
|
0.700 | GeneticVariation | UNIPROT | Mutations in a novel gene, NPHP3, cause adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis. | 12872122 | 2003 | |||||||
|
|
|
0.700 | GeneticVariation | UNIPROT | ||||||||||
|
|
|
0.700 | GeneticVariation | UNIPROT | Mutations in a novel gene, NPHP3, cause adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis. | 12872122 | 2003 | |||||||
|
|
|
0.700 | GeneticVariation | UNIPROT | ||||||||||
|
|
|
0.700 | GeneticVariation | UNIPROT | Mutations in a novel gene, NPHP3, cause adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis. | 12872122 | 2003 | |||||||
|
|
|
0.010 | GeneticVariation | BEFREE | Liver involvement was observed in all patients with NPHP3 mutations and congenital heart disease in two patients harbouring NPHP3 mutation of c.2369 T > C (p.L790P). | 26184788 | 2016 | |||||||
|
|
|
A | 0.700 | CausalMutation | CLINVAR | |||||||||
|
|
|
A | 0.700 | CausalMutation | CLINVAR | |||||||||
|
|
|
A | 0.700 | CausalMutation | CLINVAR | |||||||||
|
|
|
A | 0.700 | CausalMutation | CLINVAR | |||||||||
|
|
|
A | 0.700 | CausalMutation | CLINVAR | |||||||||
|
|
|
A | 0.700 | CausalMutation | CLINVAR | |||||||||
|
|
|
A | 0.700 | CausalMutation | CLINVAR | |||||||||
|
|
|
A | 0.700 | CausalMutation | CLINVAR | |||||||||
|
|
|
A | 0.700 | CausalMutation | CLINVAR | Mutations of NPHP2 and NPHP3 in infantile nephronophthisis. | 19177160 | 2009 | ||||||
|
|
|
A | 0.700 | CausalMutation | CLINVAR | Lethal cystic kidney disease in Amish neonates associated with homozygous nonsense mutation of NPHP3. | 19303681 | 2009 | ||||||
|
|
|
A | 0.700 | CausalMutation | CLINVAR | |||||||||
|
|
|
A | 0.700 | CausalMutation | CLINVAR | Homozygous mutation in the NPHP3 gene causing foetal nephronophthisis. | 28921755 | 2017 | ||||||
|
|
|
A | 0.700 | CausalMutation | CLINVAR | |||||||||
|
|
|
AT | 0.700 | CausalMutation | CLINVAR | |||||||||
|
|
|
C | 0.700 | CausalMutation | CLINVAR | |||||||||
|
|
|
C | 0.700 | CausalMutation | CLINVAR | |||||||||
|
|
|
C | 0.700 | CausalMutation | CLINVAR |