{{Rsnum
|rsid=386833957
|Chromosome=19
|Orientation=minus
|geno1=(-;-)
|geno2=(-;AG)
|geno3=(AG;AG)
|Gene=NPHS1
|position=35849600
|Gene_s=NPHS1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G
|CHROM=19
|CLNACC=RCV000049932.1
|CLNALLE=1
|CLNDBN=Finnish congenital nephrotic syndrome
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0403399:256300:839:197601003
|CLNHGVS=NC_000019.9:g.36340502_36340503delCT
|CLNSIG=4
|Disease=Finnish congenital nephrotic syndrome
|FwdREF=AG
|REF=GCT
|RSPOS=36340501
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050068000000000002110200
|WGT=0
|dbSNPBuildID=137
|rsid=386833957
|GENEINFO=NPHS1:4868
|GENE_ID=4868
|GENE_NAME=NPHS1
}}{{PMID Auto
|PMID=11854170
|Title=Genotype/phenotype correlations of NPHS1 and NPHS2 mutations in nephrotic syndrome advocate a functional inter-relationship in glomerular filtration.
}}