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rs10875943

From SNPedia

Orientationplus
Stabilizedplus
Make rs10875943(C;C)
Make rs10875943(C;T)
Make rs10875943(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position49282227
is asnp
is mentioned by
dbSNPrs10875943
ebirs10875943
HLIrs10875943
Exacrs10875943
Varsomers10875943
Maprs10875943
PheGenIrs10875943
hapmaprs10875943
1000 genomesrs10875943
hgdprs10875943
ensemblrs10875943
gopubmedrs10875943
geneviewrs10875943
scholarrs10875943
googlers10875943
pharmgkbrs10875943
gwascentralrs10875943
openSNPrs10875943
23andMers10875943
23andMe allrs10875943
SNP Nexus

SNPshotrs10875943
SNPdbers10875943
MSV3drs10875943
GWAS Ctlgrs10875943
GMAF0.4656
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21743467OA-icon.png]
Trait
Title Seven prostate cancer susceptibility loci identified by a multi-stage genome-wide association study.
Risk Allele C
P-val 7E-12
Odds Ratio 1.0700 [1.04-1.10]