{{Rsnum
|rsid=193922609
|Chromosome=3
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=VHL
|position=10142167
|Gene_s=VHL
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=193922609
|Reversed=0
|FwdREF=G
|FwdALT=C
|REF=G
|ALT=C
|RSPOS=10183851
|CHROM=3
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050268000000000002100100
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.10183851G>C
|CLNSRC=Correlagen
|CLNORIGIN=1
|CLNSIG=4
|CLNDBN=Von Hippel-Lindau syndrome
|Disease=Von Hippel-Lindau syndrome
|Tags=PM;PMC;S3D;OTHERKG;LSD
|CLNACC=RCV000030583.1
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1463:C0019562:193300:892:46659004
|GENEINFO=VHL:7428
|GENE_ID=7428
|GENE_NAME=VHL
}}{{PMID Auto
|PMID=9829911
|Title=Improved detection of germline mutations in the von Hippel-Lindau disease tumor suppressor gene.
}}

{{PMID Auto
|PMID=12624160
|Title=High frequency of novel germline mutations in the VHL gene in the heterogeneous population of Brazil.
|OA=1
}}

{{PMID Auto
|PMID=18836774
|Title=Computational detection of deleterious SNPs and their effect on sequence and structural level of the VHL gene.
}}