{{Rsnum
|rsid=104893824
|Chromosome=3
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=VHL
|position=10142181
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=VHL
}}{{omim
|id=608537
|rsnum=104893824
|variant=0017
}}
{{omim
|id=608537
|rsnum=104893824
|variant=0012
}}{{ClinVar
|rsid=104893824
|Reversed=0
|FwdREF=T
|FwdALT=A,C
|REF=T
|ALT=A,C
|RSPOS=10183865
|CHROM=3
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=VHL:7428
|GENE_NAME=VHL
|GENE_ID=7428
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000003.11:g.10183865T>A; NC_000003.11:g.10183865T>C
|CLNORIGIN=1
|CLNSRCID=
608537.0017; 608537.0012
|CLNSIG=5
|CLNCUI=
|CLNACC=
RCV000002316.1; RCV000002308.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDBN=Von Hippel-Lindau syndrome
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1463:C0019562:193300:892:46659004
|CLNSRC=OMIM Allelic Variant
|Disease=Von Hippel-Lindau syndrome
}}