{{Rsnum
|rsid=267606918
|Chromosome=19
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=NPHS1
|position=35842421
|Gene_s=NPHS1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=19
|CLNACC=RCV000007278.1
|CLNALLE=1
|CLNDBN=Finnish congenital nephrotic syndrome
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0403399:256300:839:197601003
|CLNHGVS=NC_000019.9:g.36333323C>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=602716.0009
|Disease=Finnish congenital nephrotic syndrome
|FwdALT=A
|FwdREF=G
|GENEINFO=NPHS1:4868
|GENE_ID=4868
|GENE_NAME=NPHS1
|REF=C
|RSPOS=36333323
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050260000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=267606918
}}