{{Rsnum
|rsid=200253809
|Gene=NPHS1
|Chromosome=19
|position=35844249
|Orientation=plus
|GMAF=0.001377
|Gene_s=NPHS1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ClinVar
|ALT=A,C
|CAF=0.9986; 0.001377; .
|CHROM=19
|CLNACC=RCV000049874.1
|CLNALLE=2
|CLNDBN=Finnish congenital nephrotic syndrome
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0403399:256300:839:197601003
|CLNHGVS=NC_000019.9:g.36335151G>C
|CLNSIG=4
|COMMON=0
|Disease=Finnish congenital nephrotic syndrome
|FwdALT=A,C
|FwdREF=G
|GENEINFO=NPHS1:4868
|GENE_ID=4868
|GENE_NAME=NPHS1
|REF=G
|RSPOS=36335151
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;KGPhase1;KGPROD;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050068000000000016110100
|WGT=0
|dbSNPBuildID=137
|rsid=200253809
}}{{PMID Auto
|PMID=18614772
|Title=Nephrin mutations can cause childhood-onset steroid-resistant nephrotic syndrome.
|OA=1
}}