Rs10788160

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Orientationplus
Make rs10788160(A;A)
Make rs10788160(A;G)
Make rs10788160(G;G)
ReferenceGRCh37 37.1/132
Chromosome10
Position123033549
is asnp
is mentioned by
dbSNPrs10788160
Exacrs10788160
PheGenIrs10788160
nextbiors10788160
hapmaprs10788160
1000 genomesrs10788160
hgdprs10788160
ensemblrs10788160
gopubmedrs10788160
geneviewrs10788160
scholarrs10788160
googlers10788160
pharmgkbrs10788160
gwascentralrs10788160
openSNPrs10788160
23andMers10788160
23andMe allrs10788160
SNP Nexus

SNPshotrs10788160
SNPdbers10788160
MSV3drs10788160
GMAF0.174
? (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 5E-15
Odds Ratio 10.2000 [NR] % increase


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


[PMID 24345439] Prostate cancer risk alleles are associated with prostate cancer tumor volume and prostate size


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