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rs11067228

From SNPedia

Orientationplus
Stabilizedplus
Make rs11067228(A;A)
Make rs11067228(A;G)
Make rs11067228(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position114656455
is asnp
is mentioned by
dbSNPrs11067228
dbSNP (classic)rs11067228
ClinGenrs11067228
ebirs11067228
HLIrs11067228
Exacrs11067228
Gnomadrs11067228
Varsomers11067228
LitVarrs11067228
Maprs11067228
PheGenIrs11067228
Biobankrs11067228
1000 genomesrs11067228
hgdprs11067228
ensemblrs11067228
geneviewrs11067228
scholarrs11067228
googlers11067228
pharmgkbrs11067228
gwascentralrs11067228
openSNPrs11067228
23andMers11067228
SNPshotrs11067228
SNPdbers11067228
MSV3drs11067228
GWAS Ctlgrs11067228
GMAF0.3618
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GWAS snp
PMID [PMID 21160077OA-icon.png]
Trait
Title Genetic Correction of PSA Values Using Sequence Variants Associated with PSA Levels
Risk Allele A
P-val 2E-11
Odds Ratio 8.3000 [NR] % increase

Prostate-Specific Antigen


[PMID 23937305OA-icon.png] Validation of association of genetic variants at 10q with prostate-specific antigen (PSA) levels in men at high risk for prostate cancer


[PMID 23246478OA-icon.png] Personalized prostate specific antigen testing using genetic variants may reduce unnecessary prostate biopsies.