Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10518133
rs10518133
PARM1
A 0.700 GeneticVariation GWASCAT Genetic Identification of Two Novel Loci Associated with Steroid-Sensitive Nephrotic Syndrome. 31263063

2019
dbSNP: rs201899638
rs201899638
PTPRD
0.700 GeneticVariation GWASCAT Genetic Identification of Two Novel Loci Associated with Steroid-Sensitive Nephrotic Syndrome. 31263063

2019
dbSNP: rs2637678
rs2637678 		0.700 GeneticVariation GWASCAT Genetic Identification of Two Novel Loci Associated with Steroid-Sensitive Nephrotic Syndrome. 31263063

2019
dbSNP: rs2746419
rs2746419
AHI1
A 0.700 GeneticVariation GWASCAT Genetic Identification of Two Novel Loci Associated with Steroid-Sensitive Nephrotic Syndrome. 31263063

2019
dbSNP: rs2858317
rs2858317 		0.700 GeneticVariation GWASCAT Genetic Identification of Two Novel Loci Associated with Steroid-Sensitive Nephrotic Syndrome. 31263063

2019
dbSNP: rs487575
rs487575
LOC105374264
0.700 GeneticVariation GWASCAT Genetic Identification of Two Novel Loci Associated with Steroid-Sensitive Nephrotic Syndrome. 31263063

2019
dbSNP: rs9273542
rs9273542
HLA-DQB1 ; HLA-DQB1-AS1
T 0.700 GeneticVariation GWASCAT Genetic Identification of Two Novel Loci Associated with Steroid-Sensitive Nephrotic Syndrome. 31263063

2019
dbSNP: rs1063348
rs1063348
HLA-DQB1 ; HLA-DQB1-AS1
G 0.700 GeneticVariation GWASCAT Transethnic, Genome-Wide Analysis Reveals Immune-Related Risk Alleles and Phenotypic Correlates in Pediatric Steroid-Sensitive Nephrotic Syndrome. 29903748

2018
dbSNP: rs28366266
rs28366266
HLA-DRB1
C 0.700 GeneticVariation GWASCAT Transethnic, Genome-Wide Analysis Reveals Immune-Related Risk Alleles and Phenotypic Correlates in Pediatric Steroid-Sensitive Nephrotic Syndrome. 29903748

2018
dbSNP: rs2858829
rs2858829 		0.700 GeneticVariation GWASCAT Transethnic, Genome-Wide Analysis Reveals Immune-Related Risk Alleles and Phenotypic Correlates in Pediatric Steroid-Sensitive Nephrotic Syndrome. 29903748

2018
dbSNP: rs4642516
rs4642516 		T 0.700 GeneticVariation GWASCAT Strong Association of the HLA-DR/DQ Locus with Childhood Steroid-Sensitive Nephrotic Syndrome in the Japanese Population. 30012571

2018
dbSNP: rs59882675
rs59882675
BTC
0.700 GeneticVariation GWASCAT Transethnic, Genome-Wide Analysis Reveals Immune-Related Risk Alleles and Phenotypic Correlates in Pediatric Steroid-Sensitive Nephrotic Syndrome. 29903748

2018
dbSNP: rs9348883
rs9348883
HCG23 ; TSBP1-AS1
T 0.700 GeneticVariation GWASCAT Transethnic, Genome-Wide Analysis Reveals Immune-Related Risk Alleles and Phenotypic Correlates in Pediatric Steroid-Sensitive Nephrotic Syndrome. 29903748

2018
dbSNP: rs119473033
rs119473033
SMARCAL1
T 0.700 CausalMutation CLINVAR A novel SMARCAL1 mutation associated with a mild phenotype of Schimke immuno-osseous dysplasia (SIOD). 24589093

2014
dbSNP: rs16946160
rs16946160
GPC5
A 0.700 GeneticVariation GWASCAT Common variation in GPC5 is associated with acquired nephrotic syndrome. 21441931

2011
dbSNP: rs119473033
rs119473033
SMARCAL1
T 0.700 CausalMutation CLINVAR Schimke immuno-osseous dysplasia: SMARCAL1 loss-of-function and phenotypic correlation. 18805831

2009
dbSNP: rs267606919
rs267606919
NPHS1
A 0.700 CausalMutation CLINVAR Thirteen novel NPHS1 mutations in a large cohort of children with congenital nephrotic syndrome. 18503012

2008
dbSNP: rs267606919
rs267606919
NPHS1
A 0.700 CausalMutation CLINVAR Recurrence of proteinuria following renal transplantation in congenital nephrotic syndrome of the Finnish type. 16518627

2006
dbSNP: rs28940578
rs28940578
MEFV
T 0.700 CausalMutation CLINVAR The spectrum of familial Mediterranean fever gene mutations in Arabs: report of a large series. 15942916

2005
dbSNP: rs119473033
rs119473033
SMARCAL1
T 0.700 CausalMutation CLINVAR Mutant chromatin remodeling protein SMARCAL1 causes Schimke immuno-osseous dysplasia. 11799392

2002
dbSNP: rs267606919
rs267606919
NPHS1
A 0.700 CausalMutation CLINVAR Genotypephenotype correlations of NPHS1 and NPHS2 mutations in nephrotic syndrome advocate a functional inter-relationship in glomerular filtration. 11854170

2002
dbSNP: rs1569504068
rs1569504068
COL4A5
A 0.700 GeneticVariation CLINVAR

dbSNP: rs199840952
rs199840952
ZAP70
T 0.700 CausalMutation CLINVAR

dbSNP: rs267606954
rs267606954
PLCE1
T 0.700 CausalMutation CLINVAR

dbSNP: rs869025224
rs869025224
ZAP70
C 0.700 CausalMutation CLINVAR