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rs7579899

From SNPedia

Orientationplus
Stabilizedplus
Make rs7579899(A;A)
Make rs7579899(A;G)
Make rs7579899(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position46310465
GeneEPAS1
is asnp
is mentioned by
dbSNPrs7579899
ebirs7579899
HLIrs7579899
Exacrs7579899
Varsomers7579899
Maprs7579899
PheGenIrs7579899
hapmaprs7579899
1000 genomesrs7579899
hgdprs7579899
ensemblrs7579899
gopubmedrs7579899
geneviewrs7579899
scholarrs7579899
googlers7579899
pharmgkbrs7579899
gwascentralrs7579899
openSNPrs7579899
23andMers7579899
23andMe allrs7579899
SNP Nexus

SNPshotrs7579899
SNPdbers7579899
MSV3drs7579899
GWAS Ctlgrs7579899
GMAF0.4389
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 21131975OA-icon.png]
Trait
Title Genome-wide association study of renal cell carcinoma identifies two susceptibility loci on 2p21 and 11q13.3
Risk Allele
P-val 2E-9
Odds Ratio 1.1500 [1.10-1.21]

23andMe reports that rs7579899(A,A) homozygotes are 1.15 times more likely, and (G,G) homozygotes 1.15 times less likely, than (A,G) heterozygotes to develop renal cell carcinoma (a form of kidney cancer). [PMID 21131975OA-icon.png]


[PMID 22131124] Chromosome 11q13.3 variant modifies renal cell cancer risk in a Chinese population


[PMID 22113997OA-icon.png] The chromosome 2p21 region harbors a complex genetic architecture for association with risk for renal cell carcinoma