Have questions? Visit https://www.reddit.com/r/SNPedia

rs5759167

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 2 Higher prostate cancer risk
Make rs5759167(G;G)
Make rs5759167(G;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position43104206
is asnp
is mentioned by
dbSNPrs5759167
ebirs5759167
HLIrs5759167
Exacrs5759167
Varsomers5759167
Maprs5759167
PheGenIrs5759167
hapmaprs5759167
1000 genomesrs5759167
hgdprs5759167
ensemblrs5759167
gopubmedrs5759167
geneviewrs5759167
scholarrs5759167
googlers5759167
pharmgkbrs5759167
gwascentralrs5759167
openSNPrs5759167
23andMers5759167
23andMe allrs5759167
SNP Nexus

SNPshotrs5759167
SNPdbers5759167
MSV3drs5759167
GWAS Ctlgrs5759167
GMAF0.3705
Max Magnitude2
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 19767753OA-icon.png]
Trait Prostate cancer
Title Identification of seven new prostate cancer susceptibility loci through a genome-wide association study
Risk Allele T
P-val 6E-29
Odds Ratio 1.16 [1.14-1.20]


[PMID 21820706OA-icon.png] Prostate Cancer Risk Alleles and Their Associations With Other Malignancies


[PMID 21390317OA-icon.png] Characterizing associations and SNP-environment interactions for GWAS-identified prostate cancer risk markers--results from BPC3.


GET Evidence
rs5759167
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.351562
summary



[PMID 23405784] [Susceptibility to prostate cancer in Han Chinese: single nucleotide polymorphism analysis of 1 667 cases]