{{Rsnum
|rsid=137853042
|Chromosome=19
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=NPHS1
|position=35831358
|Gene_s=NPHS1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=602716
|variant=0002
|rsnum=137853042
}}{{ClinVar
|rsid=137853042
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=36322260
|CHROM=19
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=NPHS1:4868
|GENE_NAME=NPHS1
|GENE_ID=4868
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000019.9:g.36322260G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=602716.0002
|CLNSIG=5
|CLNCUI=C0403399
|CLNDBN=Finnish congenital nephrotic syndrome
|Disease=Finnish congenital nephrotic syndrome
|CLNACC=RCV000007270.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0403399:256300:839:197601003
}}