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rs902774

From SNPedia

Orientationplus
Stabilizedplus
Make rs902774(A;A)
Make rs902774(A;G)
Make rs902774(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position52880120
is asnp
is mentioned by
dbSNPrs902774
ebirs902774
HLIrs902774
Exacrs902774
Varsomers902774
Maprs902774
PheGenIrs902774
hapmaprs902774
1000 genomesrs902774
hgdprs902774
ensemblrs902774
gopubmedrs902774
geneviewrs902774
scholarrs902774
googlers902774
pharmgkbrs902774
gwascentralrs902774
openSNPrs902774
23andMers902774
23andMe allrs902774
SNP Nexus

SNPshotrs902774
SNPdbers902774
MSV3drs902774
GWAS Ctlgrs902774
GMAF0.09642
Max Magnitude
? (A;A) (A;G) (G;G) 28
Rs902774
PubMed [PMID 18264097]
Affy Probeset SNP_A-8629651
Affy Orientation reverse
On GW 5.0 0
Alleles A/B C/T
Ancestral G
Population UK, Australia
Allele A
Case Freq. 0.18
Control Freq. 0.14
Odds Ratio Het 1.34
Odds Ratio Hom 2.29
Odds Ratio All
Disease Prostate cancer (PC)


rs902774 increases susceptibility to Prostate cancer 1.34 times for heterozygotes (AG) and 2.29 times for homozygotes (AA) [PMID 18264097]

GWAS snp
PMID [PMID 21743057OA-icon.png]
Trait
Title Genome-wide association study identifies new prostate cancer susceptibility loci.
Risk Allele A
P-val 5E-9
Odds Ratio 1.1700 [1.11-1.24]

[PMID 19639606OA-icon.png] Correcting "winner's curse" in odds ratios from genomewide association findings for major complex human diseases.


[PMID 23405784] [Susceptibility to prostate cancer in Han Chinese: single nucleotide polymorphism analysis of 1 667 cases]