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rs1314913

From SNPedia

Orientationplus
Stabilizedplus
Make rs1314913(C;C)
Make rs1314913(C;T)
Make rs1314913(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position68232877
GeneRAD51B
is asnp
is mentioned by
dbSNPrs1314913
ebirs1314913
HLIrs1314913
Exacrs1314913
Varsomers1314913
Maprs1314913
PheGenIrs1314913
hapmaprs1314913
1000 genomesrs1314913
hgdprs1314913
ensemblrs1314913
gopubmedrs1314913
geneviewrs1314913
scholarrs1314913
googlers1314913
pharmgkbrs1314913
gwascentralrs1314913
openSNPrs1314913
23andMers1314913
23andMe allrs1314913
SNP Nexus

SNPshotrs1314913
SNPdbers1314913
MSV3drs1314913
GWAS Ctlgrs1314913
GMAF0.1084
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23001122OA-icon.png]
Trait Breast cancer (male)
Title Genome-wide association study identifies a common variant in RAD51B associated with male breast cancer risk.
Risk Allele
P-val 3E-13
Odds Ratio 1.57 [1.39-1.77]


[PMID 17903304OA-icon.png] Framingham Heart Study 100K project: genome-wide associations for cardiovascular disease outcomes.


[PMID 17903306OA-icon.png] Genome-wide association study of electrocardiographic and heart rate variability traits: the Framingham Heart Study.


[PMID 26248686] Novel and known genetic variants for male breast cancer risk at 8q24.21, 9p21.3, 11q13.3 and 14q24.1: Results from a multicenter study in Italy