{{Rsnum
|rsid=121907900
|Chromosome=11
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=WT1
|position=32392020
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=WT1
}}{{omim
|id=607102
|rsnum=121907900
|variant=0003
}}{{ClinVar
|rsid=121907900
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=32413566
|CHROM=11
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=WT1:7490
|GENE_NAME=WT1
|GENE_ID=7490
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.32413566G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=607102.0003
|CLNSIG=5
|CLNCUI=C0950121; C1837026
|CLNDBN=Drash syndrome; Meacham syndrome; Diffuse mesangial sclerosis
|Disease=Drash syndrome; Meacham syndrome; Diffuse mesangial sclerosis
|CLNACC=RCV000003656.1; RCV000003657.1; RCV000003658.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT; MedGen:OMIM:Orphanet; MedGen:OMIM:Orphanet:SNOMED_CT:SNOMED_CT
|CLNDSDBID=C0950121:194080:220:236385009; C1837026:608978:3097; C0268747:256370:656:111406002:236383002
}}