Condition: Nephrotic Syndrome


rs2746419 in AHI1 gene and Nephrotic Syndrome PMID 31263063 2019 Genetic Identification of Two Novel Loci Associated with Steroid-Sensitive Nephrotic Syndrome.

rs59882675 in BTC gene and Nephrotic Syndrome PMID 29903748 2018 Transethnic, Genome-Wide Analysis Reveals Immune-Related Risk Alleles and Phenotypic Correlates in Pediatric Steroid-Sensitive Nephrotic Syndrome.

rs16946160 in GPC5 gene and Nephrotic Syndrome PMID 21441931 2011 Common variation in GPC5 is associated with acquired nephrotic syndrome.

rs1063348 in HLA-DQB1-AS1;HLA-DQB1 gene and Nephrotic Syndrome PMID 29903748 2018 Transethnic, Genome-Wide Analysis Reveals Immune-Related Risk Alleles and Phenotypic Correlates in Pediatric Steroid-Sensitive Nephrotic Syndrome.

rs9273542 in HLA-DQB1;HLA-DQB1-AS1 gene and Nephrotic Syndrome PMID 31263063 2019 Genetic Identification of Two Novel Loci Associated with Steroid-Sensitive Nephrotic Syndrome.

rs28366266 in HLA-DRB1 gene and Nephrotic Syndrome PMID 29903748 2018 Transethnic, Genome-Wide Analysis Reveals Immune-Related Risk Alleles and Phenotypic Correlates in Pediatric Steroid-Sensitive Nephrotic Syndrome.

rs487575 in LOC105374264 gene and Nephrotic Syndrome PMID 31263063 2019 Genetic Identification of Two Novel Loci Associated with Steroid-Sensitive Nephrotic Syndrome.

rs28940578 in MEFV gene and Nephrotic Syndrome PMID 15942916 2005 The spectrum of familial Mediterranean fever gene mutations in Arabs: report of a large series.

rs267606919 in NPHS1 gene and Nephrotic Syndrome PMID 16518627 2006 Recurrence of proteinuria following renal transplantation in congenital nephrotic syndrome of the Finnish type.

PMID 18503012 2008 Thirteen novel NPHS1 mutations in a large cohort of children with congenital nephrotic syndrome.

PMID 11854170 2002 Genotypephenotype correlations of NPHS1 and NPHS2 mutations in nephrotic syndrome advocate a functional inter-relationship in glomerular filtration.

rs10518133 in PARM1 gene and Nephrotic Syndrome PMID 31263063 2019 Genetic Identification of Two Novel Loci Associated with Steroid-Sensitive Nephrotic Syndrome.

rs201899638 in PTPRD gene and Nephrotic Syndrome PMID 31263063 2019 Genetic Identification of Two Novel Loci Associated with Steroid-Sensitive Nephrotic Syndrome.

rs119473033 in SMARCAL1 gene and Nephrotic Syndrome PMID 11799392 2002 Mutant chromatin remodeling protein SMARCAL1 causes Schimke immuno-osseous dysplasia.

PMID 18805831 2009 Schimke immuno-osseous dysplasia: SMARCAL1 loss-of-function and phenotypic correlation.

PMID 24589093 2014 A novel SMARCAL1 mutation associated with a mild phenotype of Schimke immuno-osseous dysplasia (SIOD).

rs9348883 in TSBP1-AS1;HCG23 gene and Nephrotic Syndrome PMID 29903748 2018 Transethnic, Genome-Wide Analysis Reveals Immune-Related Risk Alleles and Phenotypic Correlates in Pediatric Steroid-Sensitive Nephrotic Syndrome.