Variant: rs1244884053 

    present in Gene: NPHS1
    present in Chromosome: 19
    Position on Chromosome: 35842244
    Alleles of this Variant: TTAG/-

rs1244884053 in NPHS1 gene and Finnish congenital nephrotic syndrome PMID 26668027 2016 Rapid Response to Cyclosporin A and Favorable Renal Outcome in Nongenetic Versus Genetic Steroid-Resistant Nephrotic Syndrome.

PMID 19812541 2009 Nephrin mutations cause childhood- and adult-onset focal segmental glomerulosclerosis.