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rs11199874

From SNPedia

Orientationplus
Stabilizedplus
Make rs11199874(A;A)
Make rs11199874(A;G)
Make rs11199874(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position121273005
is asnp
is mentioned by
dbSNPrs11199874
ebirs11199874
HLIrs11199874
Exacrs11199874
Varsomers11199874
Maprs11199874
PheGenIrs11199874
hapmaprs11199874
1000 genomesrs11199874
hgdprs11199874
ensemblrs11199874
gopubmedrs11199874
geneviewrs11199874
scholarrs11199874
googlers11199874
pharmgkbrs11199874
gwascentralrs11199874
openSNPrs11199874
23andMers11199874
23andMe allrs11199874
SNP Nexus

SNPshotrs11199874
SNPdbers11199874
MSV3drs11199874
GWAS Ctlgrs11199874
GMAF0.214
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 22130093OA-icon.png]
Trait
Title New variants at 10q26 and 15q21 are associated with aggressive prostate cancer in a genome-wide association study from a prostate biopsy screening cohort.
Risk Allele
P-val 3E-10
Odds Ratio None None


[PMID 22523086OA-icon.png] Gene variants in the angiogenesis pathway and prostate cancer.