{{Rsnum
|rsid = 28942089
|Gene = WT1
|geno1 = (C;C)
|geno2 = (C;T)
|geno3 = (T;T)
|Orientation=minus
|ReferenceAllele=C
|MissenseAllele=T
|Chromosome=11
|position=32392672
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=WT1
}}{{omim
|desc=DENYS-DRASH SYNDROME
|id=607102
|rsnum=28942089
|variant=0012
}}
{{omim
| id = 607102
| variant = 0021
| desc    = MESANGIAL SCLEROSIS, ISOLATED DIFFUSE
| rsnum   = 28942089
}}
{{ neighbor
| rsid = 28941777
| distance = 619
}}{{ClinVar
|rsid=28942089
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=32414218
|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.32414218G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=607102.0012; 607102.0021
|CLNSIG=5
|CLNCUI=C0950121
|CLNDBN=Drash syndrome; Diffuse mesangial sclerosis
|Disease=Drash syndrome; Diffuse mesangial sclerosis
|CLNACC=RCV000003667.1; RCV000003668.1
|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 v4}}