rs902774

Orientation

plus

Stabilized

plus

Make rs902774(A;A)

Make rs902774(A;G)

Make rs902774(G;G)

Reference

GRCh38 38.1/141

Chromosome

12

Position

52880120

is a	snp
is	mentioned by
dbSNP	rs902774
dbSNP (classic)	rs902774
ClinGen	rs902774
ebi	rs902774
HLI	rs902774
Exac	rs902774
Gnomad	rs902774
Varsome	rs902774
LitVar	rs902774
Map	rs902774
PheGenI	rs902774
Biobank	rs902774
1000 genomes	rs902774
hgdp	rs902774
ensembl	rs902774
geneview	rs902774
scholar	rs902774
google	rs902774
pharmgkb	rs902774
gwascentral	rs902774
openSNP	rs902774
23andMe	rs902774
SNPshot	rs902774
SNPdbe	rs902774
MSV3d	rs902774
GWAS Ctlg	rs902774

GMAF

0.09642

Max Magnitude

0

?	(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 21743057]
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 19639606] 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]