{{Rsnum
|rsid=193922608
|Chromosome=3
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=VHL
|position=10142089
|Gene_s=VHL
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=193922608
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=10183773
|CHROM=3
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050268000000000002100100
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.10183773C>T
|CLNSRC=Correlagen
|CLNORIGIN=1
|CLNSIG=4
|CLNDBN=Von Hippel-Lindau syndrome
|Disease=Von Hippel-Lindau syndrome
|Tags=PM;PMC;S3D;OTHERKG;LSD
|CLNACC=RCV000030582.1
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1463:C0019562:193300:892:46659004
|GENEINFO=VHL:7428
|GENE_ID=7428
|GENE_NAME=VHL
}}{{PMID|17102082}} Genetic mutation screening in an italian cohort of nonsyndromic pheochromocytoma/paraganglioma patients.