{{Rsnum
|rsid=386833937
|Chromosome=19
|Orientation=minus
|geno1=(-;-)
|geno2=(-;GG)
|geno3=(GG;GG)
|Gene=NPHS1
|position=35831325
|Gene_s=NPHS1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=TCC
|CHROM=19
|CLNACC=RCV000049911.1
|CLNALLE=1
|CLNDBN=Finnish congenital nephrotic syndrome
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0403399:256300:839:197601003
|CLNHGVS=NC_000019.9:g.36322228_36322229dupCC
|CLNSIG=4
|Disease=Finnish congenital nephrotic syndrome
|FwdALT=GG
|REF=T
|RSPOS=36322227
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050068000000000002110200
|WGT=0
|dbSNPBuildID=137
|rsid=386833937
|GENEINFO=NPHS1:4868
|GENE_ID=4868
|GENE_NAME=NPHS1
}}{{PMID Auto
|PMID=11317351
|Title=Mutation spectrum in the nephrin gene (NPHS1) in congenital nephrotic syndrome.
}}