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rs1002979

From SNPedia

Orientationplus
Stabilizedplus
Make rs1002979(C;C)
Make rs1002979(C;T)
Make rs1002979(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position112779033
is asnp
is mentioned by
dbSNPrs1002979
ebirs1002979
HLIrs1002979
Exacrs1002979
Varsomers1002979
Maprs1002979
PheGenIrs1002979
hapmaprs1002979
1000 genomesrs1002979
hgdprs1002979
ensemblrs1002979
gopubmedrs1002979
geneviewrs1002979
scholarrs1002979
googlers1002979
pharmgkbrs1002979
gwascentralrs1002979
openSNPrs1002979
23andMers1002979
23andMe allrs1002979
SNP Nexus

SNPshotrs1002979
SNPdbers1002979
MSV3drs1002979
GWAS Ctlgrs1002979
GMAF0.4298
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 0.000003
Odds Ratio 1.5873 None