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rs9567349

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs9567349(A;G)
Make rs9567349(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position44063269
is asnp
is mentioned by
dbSNPrs9567349
ebirs9567349
HLIrs9567349
Exacrs9567349
Varsomers9567349
Maprs9567349
PheGenIrs9567349
hapmaprs9567349
1000 genomesrs9567349
hgdprs9567349
ensemblrs9567349
gopubmedrs9567349
geneviewrs9567349
scholarrs9567349
googlers9567349
pharmgkbrs9567349
gwascentralrs9567349
openSNPrs9567349
23andMers9567349
23andMe allrs9567349
SNP Nexus

SNPshotrs9567349
SNPdbers9567349
MSV3drs9567349
GWAS Ctlgrs9567349
GMAF0.1621
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 22219177OA-icon.png]
Trait
Title A genome-wide search for loci interacting with known prostate cancer risk-associated genetic variants.
Risk Allele
P-val 0.000004
Odds Ratio 1.6393 None