{{Rsnum
|rsid=74315348
|Gene=NPHS2
|Chromosome=1
|position=179552605
|Orientation=minus
|GMAF=0.0004591
|Gene_s=C1orf125,NPHS2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{omim
|id=604766
|rsnum=74315348
|variant=0010
}}{{ClinVar
|rsid=74315348
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=179552605
|CHROM=1
|GMAF=0.0005
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260080a05000016110100
|GENEINFO=NPHS2:7827; AXDND1:126859
|GENE_NAME=NPHS2; AXDND1
|GENE_ID=7827; 126859
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.179552605G>A
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_014625.2:c.871C>T; NM_144696.5:c.3032-1907G>A; 604766.0010
|CLNSIG=5
|CLNCUI=C1868672
|CLNDBN=Nephrotic syndrome, idiopathic, steroid-resistant
|Disease=Nephrotic syndrome
|CLNACC=RCV000005700.1
|Tags=RV;PM;S3D;NSM;REF;INT;ASP;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9995; 0.0004591
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1868672:600995:ORPHA656
|COMMON=0
}}