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rs9757252

From SNPedia

Orientationplus
Stabilizedplus
Make rs9757252(C;C)
Make rs9757252(C;T)
Make rs9757252(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position86845328
is asnp
is mentioned by
dbSNPrs9757252
ebirs9757252
HLIrs9757252
Exacrs9757252
Varsomers9757252
Maprs9757252
PheGenIrs9757252
hapmaprs9757252
1000 genomesrs9757252
hgdprs9757252
ensemblrs9757252
gopubmedrs9757252
geneviewrs9757252
scholarrs9757252
googlers9757252
pharmgkbrs9757252
gwascentralrs9757252
openSNPrs9757252
23andMers9757252
23andMe allrs9757252
SNP Nexus

SNPshotrs9757252
SNPdbers9757252
MSV3drs9757252
GWAS Ctlgrs9757252
GMAF0.4826
Max Magnitude
? (C;C) (C;T) (T;T) 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 0.000005
Odds Ratio 1.2500 None