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rs9364554

From SNPedia

Orientationplus
Stabilizedplus
Make rs9364554(C;C)
Make rs9364554(C;T)
Make rs9364554(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position160412632
GeneSLC22A3
is asnp
is mentioned by
dbSNPrs9364554
dbSNP (classic)rs9364554
ClinGenrs9364554
ebirs9364554
HLIrs9364554
Exacrs9364554
Gnomadrs9364554
Varsomers9364554
LitVarrs9364554
Maprs9364554
PheGenIrs9364554
Biobankrs9364554
1000 genomesrs9364554
hgdprs9364554
ensemblrs9364554
geneviewrs9364554
scholarrs9364554
googlers9364554
pharmgkbrs9364554
gwascentralrs9364554
openSNPrs9364554
23andMers9364554
SNPshotrs9364554
SNPdbers9364554
MSV3drs9364554
GWAS Ctlgrs9364554
GMAF0.219
Max Magnitude0
? (C;C) (C;T) (T;T) 28


cancer-genetics these snps influence genetic risk for prostate cancer

GWAS
SNP rs9364554
PubMedID [PMID 18264097]
Condition Prostate cancer
Gene SLC22A3
Risk Allele T
pValue 6.00E-010
OR 1.17
95% CI 1.08-1.26


[PMID 19336566OA-icon.png] Replication of the 10q11 and Xp11 Prostate Cancer Risk Variants: Results from a Utah Pedigree-Based Study.



[PMID 20651075OA-icon.png] Prostate Cancer Susceptibility Variants Confer Increased Risk of Disease Progression


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


[PMID 18708398OA-icon.png] Multiple novel prostate cancer predisposition loci confirmed by an international study: the PRACTICAL Consortium.


[PMID 18794092OA-icon.png] Association of prostate cancer risk variants with clinicopathologic characteristics of the disease.


[PMID 18974127OA-icon.png] Association study of prostate cancer susceptibility variants with risks of invasive ovarian, breast, and colorectal cancer.


[PMID 19074884OA-icon.png] Interaction between single nucleotide polymorphisms in selenoprotein P and mitochondrial superoxide dismutase determines prostate cancer risk.


[PMID 19104501OA-icon.png] Prostate cancer genomics: towards a new understanding.


[PMID 19318432OA-icon.png] Generalizability of associations from prostate cancer genome-wide association studies in multiple populations.


[PMID 19366831OA-icon.png] Analysis of recently identified prostate cancer susceptibility loci in a population-based study: associations with family history and clinical features.


[PMID 19434657OA-icon.png] Individual and cumulative effect of prostate cancer risk-associated variants on clinicopathologic variables in 5,895 prostate cancer patients.


[PMID 19549807OA-icon.png] Prostate cancer risk associated loci in African Americans.


[PMID 19639606OA-icon.png] Correcting "winner's curse" in odds ratios from genomewide association findings for major complex human diseases.


[PMID 20039378OA-icon.png] Estimation of genotype relative risks from pedigree data by retrospective likelihoods.


[PMID 20569440OA-icon.png] Alterations in LMTK2, MSMB and HNF1B gene expression are associated with the development of prostate cancer.


[PMID 20690139] Meta-analysis of genome-wide and replication association studies on prostate cancer.


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


[PMID 21520160] Prostate cancer risk variants are not associated with disease progression.


[PMID 21538423OA-icon.png] Early onset prostate cancer has a significant genetic component.



[PMID 28272475OA-icon.png] SLC22A3 polymorphisms do not modify pancreatic cancer risk, but may influence overall patient survival.


[PMID 29266682OA-icon.png] Profile of common prostate cancer risk variants in an unscreened Romanian population.