{{Rsnum
|rsid=267606919
|Chromosome=19
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=NPHS1
|position=35831056
|Gene_s=NPHS1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=19
|CLNACC=RCV000007276.1
|CLNALLE=1
|CLNDBN=Finnish congenital nephrotic syndrome
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0403399:256300:839:197601003
|CLNHGVS=NC_000019.9:g.36321958G>A
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=602716.0010
|Disease=Finnish congenital nephrotic syndrome
|FwdALT=T
|FwdREF=C
|GENEINFO=NPHS1:4868
|GENE_ID=4868
|GENE_NAME=NPHS1
|REF=G
|RSPOS=36321958
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=267606919
}}