{{Rsnum
|rsid=267607170
|Chromosome=3
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=VHL
|position=10149814
|Gene_s=VHL
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G
|CHROM=3
|CLNACC=RCV000002326.1
|CLNALLE=1
|CLNDBN=Von Hippel-Lindau syndrome
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1463:C0019562:193300:892:46659004
|CLNHGVS=NC_000003.11:g.10191498A>G
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=608537.0027
|Disease=Von Hippel-Lindau syndrome
|FwdALT=G
|FwdREF=A
|GENEINFO=VHL:7428
|GENE_ID=7428
|GENE_NAME=VHL
|REF=A
|RSPOS=10191498
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;S3D;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050260000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=267607170
}}