{{Rsnum
|rsid=121907909
|Chromosome=11
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=WT1
|position=32392032
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=WT1
}}{{omim
|id=607102
|rsnum=121907909
|variant=0024
}}{{ClinVar
|rsid=121907909
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=32413578
|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.32413578G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=607102.0010; 607102.0024
|CLNSIG=5
|CLNCUI=C0950122
|CLNDBN=Wilms' tumor; Frasier syndrome
|Disease=Wilms' tumor; Frasier syndrome
|CLNACC=RCV000003666.1; RCV000030877.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:OMIM:Orphanet; MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1294:NBK1360:C0027708:194070:605982:654; C0950122:136680:347:445431000
}}