{{Rsnum
|rsid=114203578
|Chromosome=19
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=NPHS1
|position=35842480
|Gene_s=NPHS1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G,T
|CHROM=19
|CLNACC=RCV000049885.1
|CLNALLE=1
|CLNDBN=Finnish congenital nephrotic syndrome
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0403399:256300:839:197601003
|CLNHGVS=NC_000019.9:g.36333382C>G
|CLNSIG=4
|Disease=Finnish congenital nephrotic syndrome
|FwdALT=G,T
|FwdREF=C
|GENEINFO=NPHS1:4868
|GENE_ID=4868
|GENE_NAME=NPHS1
|REF=C
|RSPOS=36333382
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;S3D;KGPilot123;KGPROD;OTHERKG;LSD;OM
|VC=SNV
|VP=0x05026800000000000e110100
|WGT=0
|dbSNPBuildID=132
|rsid=114203578
}}{{PMID Auto
|PMID=9915943
|Title=Structure of the gene for congenital nephrotic syndrome of the finnish type (NPHS1) and characterization of mutations.
|OA=1
}}