{{Rsnum
|rsid = 28941778
|Gene = WT1
|Orientation=minus
|ReferenceAllele=G
|MissenseAllele=A
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Chromosome=11
|position=32392014
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=WT1
}}{{omim
|desc=DENYS-DRASH SYNDROME
|id=607102
|rsnum=28941778
|variant=0006
}}
{{omim
| id = 607102
| variant = 0023
| desc    = MESANGIAL SCLEROSIS, ISOLATED DIFFUSE
| rsnum   = 28941778
}}
{{ neighbor
| rsid = 28941779
| distance = 12
}}

{{ClinVar
|rsid=28941778
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=32413560
|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.32413560C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=607102.0006; 607102.0023
|CLNSIG=5
|CLNCUI=C0950121
|CLNDBN=Drash syndrome; Diffuse mesangial sclerosis
|Disease=Drash syndrome; Diffuse mesangial sclerosis
|CLNACC=RCV000003661.1; RCV000003662.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT; MedGen:OMIM:Orphanet:SNOMED_CT:SNOMED_CT
|CLNDSDBID=C0950121:194080:220:236385009; C0268747:256370:656:111406002:236383002
}}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}