Variant: rs386833882 

    present in Gene: KIRREL2;NPHS1
    present in Chromosome: 19
    Position on Chromosome: 35851592
    Alleles of this Variant: C/-

rs386833882 in KIRREL2;NPHS1 gene and Finnish congenital nephrotic syndrome PMID 18503012 2008 Thirteen novel NPHS1 mutations in a large cohort of children with congenital nephrotic syndrome.

PMID 20507940 2010 Genotype-phenotype correlations in non-Finnish congenital nephrotic syndrome.

PMID 22584503 2012 Mutation analysis of NPHS1 in a worldwide cohort of congenital nephrotic syndrome patients.