{{Rsnum
|rsid=386833888
|Chromosome=19
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=NPHS1
|position=35845719
|Gene_s=NPHS1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=19
|CLNACC=RCV000049859.1
|CLNALLE=1
|CLNDBN=Finnish congenital nephrotic syndrome
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0403399:256300:839:197601003
|CLNHGVS=NC_000019.9:g.36336621G>C
|CLNSIG=4
|Disease=Finnish congenital nephrotic syndrome
|FwdALT=G
|FwdREF=C
|REF=G
|RSPOS=36336621
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050068000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=386833888
|GENEINFO=NPHS1:4868
|GENE_ID=4868
|GENE_NAME=NPHS1
}}{{PMID Auto
|PMID=17413422
|Title=Misleading findings of homozygosity mapping resulting from three novel mutations in NPHS1 encoding nephrin in a highly inbred community.
}}

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