{{Rsnum
|rsid=61747728
|Gene=NPHS2
|Chromosome=1
|position=179557079
|Orientation=plus
|GMAF=0.02158
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=NPHS2
}}{{omim
|id=604766
|rsnum=61747728
|variant=0011
}}{{GET Evidence
|gene=NPHS2
|aa_change=Arg229Gln
|aa_change_short=R229Q
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs61747728
|overall_frequency_n=288
|overall_frequency_d=10758
|overall_frequency=0.0267708
|n_genomes=1
|n_genomes_annotated=0
|n_haplomes=1
|n_articles=0
|n_articles_annotated=0
|gene_in_genetests=Y
|pph2_score=0.351
|genetests_testable=Y
|nblosum100=0
|autoscore=2
|webscore=N
}}{{ClinVar
|ALT=T
|CAF=0.9784; 0.02158
|CHROM=1
|CLNACC=RCV000005701.2
|CLNALLE=1
|CLNDBN=Nephrotic syndrome, type 2, susceptibility to
|CLNHGVS=NC_000001.11:g.179557079C>T
|CLNSIG=255
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNSRCID=NM_014625.2:c.686G>A; 604766.0011
|COMMON=1
|Disease=Nephrotic syndrome
|FwdALT=T
|FwdREF=C
|GENEINFO=NPHS2:7827
|GENE_ID=7827
|GENE_NAME=NPHS2
|REF=C
|RSPOS=179557079
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;S3D;NSM;REF;INT;ASP;VLD;HD;GNO;KGPhase1;KGPilot123;KGPROD;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050260080a0514051e110100
|WGT=1
|dbSNPBuildID=129
|rsid=61747728
|CLNORIGIN=1
}}