Have questions? Visit https://www.reddit.com/r/SNPedia

rs1292011

From SNPedia

Orientationminus
Stabilizedminus
Make rs1292011(C;C)
Make rs1292011(C;T)
Make rs1292011(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position115398717
is asnp
is mentioned by
dbSNPrs1292011
ebirs1292011
HLIrs1292011
Exacrs1292011
Varsomers1292011
Maprs1292011
PheGenIrs1292011
hapmaprs1292011
1000 genomesrs1292011
hgdprs1292011
ensemblrs1292011
gopubmedrs1292011
geneviewrs1292011
scholarrs1292011
googlers1292011
pharmgkbrs1292011
gwascentralrs1292011
openSNPrs1292011
23andMers1292011
23andMe allrs1292011
SNP Nexus

SNPshotrs1292011
SNPdbers1292011
MSV3drs1292011
GWAS Ctlgrs1292011
GMAF0.3673
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 22348646OA-icon.png] Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers


[PMID 22267197OA-icon.png] Genome-wide association analysis identifies three new breast cancer susceptibility loci

GWAS snp
PMID [PMID 23535729OA-icon.png]
Trait Breast cancer
Title Large-scale genotyping identifies 41 new loci associated with breast cancer risk.
Risk Allele A
P-val 9E-22
Odds Ratio 1.09 [1.06-1.11]