{{Rsnum
|rsid = 28941779
|Gene = WT1
|Orientation=minus
|ReferenceAllele=T
|MissenseAllele=C
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Chromosome=11
|position=32392026
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=WT1
}}{{omim
|desc=FRASIER SYNDROME
|id=607102
|rsnum=28941779
|variant=0025
}}
{{ neighbor
| rsid = 28941778
| distance = 12
}}
{{ neighbor
| rsid = 28941777
| distance = 27
}}

{{ClinVar
|rsid=28941779
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=32413572
|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.32413572A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=607102.0025
|CLNSIG=5
|CLNCUI=C0950122
|CLNDBN=Frasier syndrome
|Disease=Frasier syndrome
|CLNACC=RCV000003679.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0950122:136680:347:445431000
}}

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