{{Rsnum
|rsid = 28940301
|Gene = VHL
|Orientation=plus
|ReferenceAllele=C
|MissenseAllele=G
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Chromosome=3
|position=10149894
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=VHL
}}{{omim
|desc=ERYTHROCYTOSIS, FAMILIAL, 2
|id=608537
|rsnum=28940301
|variant=0024
}}
{{ neighbor
| rsid = 28940300
| distance = 3
}}

{{ClinVar
|rsid=28940301
|Reversed=0
|FwdREF=C
|FwdALT=G
|REF=C
|ALT=G
|RSPOS=10191578
|CHROM=3
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=VHL:7428
|GENE_NAME=VHL
|GENE_ID=7428
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.10191578C>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=608537.0024
|CLNSIG=5
|CLNCUI=C1837915
|CLNDBN=Erythrocytosis, familial, 2
|Disease=Erythrocytosis
|CLNACC=RCV000002323.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1837915:263400:238557
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}