{{Rsnum
|rsid=121907905
|Chromosome=11
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=WT1
|position=32392723
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=WT1
}}{{omim
|id=607102
|rsnum=121907905
|variant=0013
}}{{ClinVar
|rsid=121907905
|Reversed=1
|FwdREF=T
|FwdALT=G
|REF=A
|ALT=C
|RSPOS=32414269
|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.32414269A>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=607102.0013
|CLNSIG=5
|CLNCUI=C0950121
|CLNDBN=Drash syndrome
|Disease=Drash syndrome
|CLNACC=RCV000003669.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0950121:194080:220:236385009
}}