{{Rsnum
|rsid=386833873
|Chromosome=19
|Orientation=minus
|geno1=(-;-)
|geno2=(-;CT)
|geno3=(CT;CT)
|Gene=NPHS1
|position=35851609
|Gene_s=NPHS1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=19
|CLNACC=RCV000049844.1
|CLNALLE=1
|CLNDBN=Finnish congenital nephrotic syndrome
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0403399:256300:839:197601003
|CLNHGVS=NC_000019.9:g.36342511_36342512delAG
|CLNSIG=5
|Disease=Finnish congenital nephrotic syndrome
|FwdREF=CT
|REF=CAG
|RSPOS=36342510
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050068000000000002110200
|WGT=0
|dbSNPBuildID=137
|rsid=386833873
|GENEINFO=NPHS1:4868
|GENE_ID=4868
|GENE_NAME=NPHS1
}}{{PMID Auto
|PMID=9660941
|Title=Positionally cloned gene for a novel glomerular protein--nephrin--is mutated in congenital nephrotic syndrome.
}}

{{PMID Auto
|PMID=9915943
|Title=Structure of the gene for congenital nephrotic syndrome of the finnish type (NPHS1) and characterization of mutations.
|OA=1
}}