{{Rsnum
|rsid=5030824
|Chromosome=3
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=VHL
|position=10149885
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=VHL
}}{{omim
|id=608537
|rsnum=5030824
|variant=0014
}}

{{ClinVar
|rsid=5030824
|Reversed=0
|FwdREF=C
|FwdALT=G
|REF=C
|ALT=G
|RSPOS=10191569
|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
|CLNHGVS=NC_000003.11:g.10191569C>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=608537.0014
|CLNSIG=5
|CLNCUI=C0019562; C1837915; C0031511
|CLNDBN=Von Hippel-Lindau syndrome; Erythrocytosis, familial, 2; Pheochromocytoma
|Disease=Von Hippel-Lindau syndrome; Erythrocytosis; Pheochromocytoma
|CLNACC=RCV000002311.1; RCV000002312.1; RCV000002313.1
|Tags=PM;S3D;SLO;GNO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; MedGen:OMIM:Orphanet; GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1463:C0019562:193300:892:46659004; C1837915:263400:238557; NBK1548:C0031511:171300:29072
}}

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