{{Rsnum
|rsid=5030818
|Chromosome=3
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=VHL
|position=10149804
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=VHL
}}{{omim
|id=608537
|rsnum=5030818
|variant=0006
}}{{ClinVar
|rsid=5030818
|Reversed=0
|FwdREF=C
|FwdALT=G,T
|REF=C
|ALT=G,T
|RSPOS=10191488
|CHROM=3
|dbSNPBuildID=113
|SSR=0
|SAO=3
|VP=0x050368000000000102110120
|GENEINFO=VHL:7428
|GENE_NAME=VHL
|GENE_ID=7428
|WGT=0
|VC=SNV
|CLNALLE=2
|CLNHGVS=NC_000003.11:g.10191488C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=608537.0006
|CLNSIG=5
|CLNCUI=C0019562
|CLNDBN=Von Hippel-Lindau syndrome; Von Hippel-Lindau
|Disease=Von Hippel-Lindau syndrome; Von Hippel-Lindau
|CLNACC=RCV000002301.1; RCV000036547.1
|Tags=PM;PMC;S3D;SLO;GNO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; MedGen
|CLNDSDBID=NBK1463:C0019562:193300:892:46659004; CN169367
}}{{PMID|192708}} Detection and semiquantitative estimation of thyroxine and diiodothyronine in liothyronine sodium.

{{PMID|7987327}} A novel mutation in the von Hippel-Lindau gene.

{{PMID|12114495|OA=1
}} Germline mutations in the von Hippel-Lindau (VHL) gene in patients from Poland: disease presentation in patients with deletions of the entire VHL gene.

{{PMID|12202531}} Retinal hemangioblastoma in von Hippel-Lindau disease: a clinical and molecular study.

{{PMID|12351569}} The pressure rises: update on the genetics of phaeochromocytoma.

{{PMID|18584357}} A novel von Hippel-Lindau point mutation presents as apparently sporadic pheochromocytoma.