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rs9311171

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs9311171(G;G)
Make rs9311171(G;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37954986
GeneCTDSPL
is asnp
is mentioned by
dbSNPrs9311171
ebirs9311171
HLIrs9311171
Exacrs9311171
Varsomers9311171
Maprs9311171
PheGenIrs9311171
hapmaprs9311171
1000 genomesrs9311171
hgdprs9311171
ensemblrs9311171
gopubmedrs9311171
geneviewrs9311171
scholarrs9311171
googlers9311171
pharmgkbrs9311171
gwascentralrs9311171
openSNPrs9311171
23andMers9311171
23andMe allrs9311171
SNP Nexus

SNPshotrs9311171
SNPdbers9311171
MSV3drs9311171
GWAS Ctlgrs9311171
GMAF0.1997
Max Magnitude0
? (G;G) (G;T) (T;T) 28
GWAS
SNP rs9311171
PubMedID [PMID 17903305OA-icon.png]
Condition Prostate cancer
Gene CTDSPL
Risk Allele
pValue 2.00E-006
OR NA
95% CI



[PMID 17903302OA-icon.png] Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness.

[PMID 17903305] A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study


GET Evidence
rs9311171
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.25
summary