{{Rsnum
|rsid=5030820
|Chromosome=3
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=VHL
|position=10149822
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=VHL
}}{{omim
|id=608537
|rsnum=5030820
|variant=0003
}}
{{omim
|id=608537
|rsnum=5030820
|variant=0004
}}

{{ClinVar
|rsid=5030820
|Reversed=0
|FwdREF=C
|FwdALT=G,T
|REF=C
|ALT=G,T
|RSPOS=10191506
|CHROM=3
|dbSNPBuildID=113
|SSR=0
|SAO=1
|VP=0x050360000000000102110100
|GENEINFO=VHL:7428
|GENE_NAME=VHL
|GENE_ID=7428
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000003.11:g.10191506C>G; NC_000003.11:g.10191506C>T
|CLNORIGIN=1
|CLNSRCID=
608537.0004; 608537.0003; 608537.0010; 608537.0011
|CLNSIG=5
|CLNCUI=
|CLNACC=
RCV000002304.1; RCV000002302.1; RCV000002303.1
|Tags=PM;S3D;SLO;GNO;OTHERKG;LSD;OM
|CLNDBN=Von Hippel-Lindau syndrome; Pheochromocytoma
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1463:C0019562:193300:892:46659004; NBK1548:C0031511:171300:29072
|CLNSRC=OMIM Allelic Variant
|Disease=Von Hippel-Lindau syndrome; Pheochromocytoma
}}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}