{{Rsnum
|rsid=386833956
|Chromosome=19
|Orientation=minus
|geno1=(CACCCCGG;CACCCCGG)
|geno2=(CACCCCGG;TT)
|geno3=(TT;TT)
|Gene=NPHS1
|position=35849641
|Gene_s=NPHS1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=TAA
|CHROM=19
|CLNACC=RCV000049931.1
|CLNALLE=1
|CLNDBN=Finnish congenital nephrotic syndrome
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0403399:256300:839:197601003
|CLNHGVS=NC_000019.9:g.36340543_36340550delCCGGGGTGinsAA
|CLNSIG=4
|Disease=Finnish congenital nephrotic syndrome
|FwdALT=TT
|FwdREF=CACCCCGG
|REF=TCCGGGGTG
|RSPOS=36340542
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050068000000000002110200
|WGT=0
|dbSNPBuildID=137
|rsid=386833956
|GENEINFO=NPHS1:4868
|GENE_ID=4868
|GENE_NAME=NPHS1
}}{{PMID Auto
|PMID=9915943
|Title=Structure of the gene for congenital nephrotic syndrome of the finnish type (NPHS1) and characterization of mutations.
|OA=1
}}

{{PMID Auto
|PMID=11854170
|Title=Genotype/phenotype correlations of NPHS1 and NPHS2 mutations in nephrotic syndrome advocate a functional inter-relationship in glomerular filtration.
}}

{{PMID Auto
|PMID=18503012
|Title=Thirteen novel NPHS1 mutations in a large cohort of children with congenital nephrotic syndrome.
|OA=1
}}

{{PMID Auto
|PMID=20172850
|Title=Nineteen novel NPHS1 mutations in a worldwide cohort of patients with congenital nephrotic syndrome (CNS).
|OA=1
}}