rs779805

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs779805(A;A)

Make rs779805(A;G)

Reference

GRCh38 38.1/141

Chromosome

3

Position

10141653

Gene

VHL

is a	snp
is	mentioned by
dbSNP	rs779805
dbSNP (classic)	rs779805
ClinGen	rs779805
ebi	rs779805
HLI	rs779805
Exac	rs779805
Gnomad	rs779805
Varsome	rs779805
LitVar	rs779805
Map	rs779805
PheGenI	rs779805
Biobank	rs779805
1000 genomes	rs779805
hgdp	rs779805
ensembl	rs779805
geneview	rs779805
scholar	rs779805
google	rs779805
pharmgkb	rs779805
gwascentral	rs779805
openSNP	rs779805
23andMe	rs779805
SNPshot	rs779805
SNPdbe	rs779805
MSV3d	rs779805
GWAS Ctlg	rs779805

GMAF

0.4164

Max Magnitude

0

?

(A;A) (A;G) (G;G)

28

[PMID 22084938] Association between VHL Single Nucleotide Polymorphism (rs779805) and the Susceptibility to Prostate Cancer in Chinese

[PMID 15696489] [Analysis of two single nucleotide polymorphisms in von Hippel-Lindau gene and detection of loss of heterozygosity in Chinese sporadic renal cell carcinoma].

[PMID 18998488] Two hypoxia sensor genes and their association with symptoms of acute mountain sickness in Sherpas.

[PMID 19996202 ] Analysis of VHL Gene Alterations and their Relationship to Clinical Parameters in Sporadic Conventional Renal Cell Carcinoma.

[PMID 21778301] The polymorphisms in the VHL and HIF1A genes are associated with the prognosis but not the development of renal cell carcinoma.

[PMID 25217002 ] Two single nucleotide polymorphisms in the von Hippel-Lindau tumor suppressor gene in Taiwanese with renal cell carcinoma

ClinVar
Risk	rs779805(A;A)
Alt	rs779805(A;A)
Reference	Rs779805(G;G)
Significance	Non-pathogenic
Disease	Von Hippel-Lindau syndrome
Variation	info
Gene	VHL
CLNDBN	Von Hippel-Lindau syndrome
Reversed	0
HGVS	NC_000003.11:g.10183337G>A
CLNSRC
CLNACC	RCV000269168.1,