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rs13264970

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;T) 0 common in complete genomics
Make rs13264970(C;C)
Make rs13264970(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position82161594
is asnp
is mentioned by
dbSNPrs13264970
ebirs13264970
HLIrs13264970
Exacrs13264970
Varsomers13264970
Maprs13264970
PheGenIrs13264970
hapmaprs13264970
1000 genomesrs13264970
hgdprs13264970
ensemblrs13264970
gopubmedrs13264970
geneviewrs13264970
scholarrs13264970
googlers13264970
pharmgkbrs13264970
gwascentralrs13264970
openSNPrs13264970
23andMers13264970
23andMe allrs13264970
SNP Nexus

SNPshotrs13264970
SNPdbers13264970
MSV3drs13264970
GWAS Ctlgrs13264970
GMAF0.4082
Max Magnitude0
? (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 0.000004
Odds Ratio 1.2987 None