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rs779805

From SNPedia

Orientationplus
Stabilizedplus
Make rs779805(A;A)
Make rs779805(A;G)
Make rs779805(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position10141653
GeneVHL
is asnp
is mentioned by
dbSNPrs779805
ebirs779805
HLIrs779805
Exacrs779805
Varsomers779805
Maprs779805
PheGenIrs779805
hapmaprs779805
1000 genomesrs779805
hgdprs779805
ensemblrs779805
gopubmedrs779805
geneviewrs779805
scholarrs779805
googlers779805
pharmgkbrs779805
gwascentralrs779805
openSNPrs779805
23andMers779805
23andMe allrs779805
SNP Nexus

SNPshotrs779805
SNPdbers779805
MSV3drs779805
GWAS Ctlgrs779805
GMAF0.4164
Max Magnitude
? (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 19996202OA-icon.png] 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 25217002OA-icon.png] Two single nucleotide polymorphisms in the von Hippel-Lindau tumor suppressor gene in Taiwanese with renal cell carcinoma