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rs12710696

From SNPedia

Orientationplus
Stabilizedplus
Make rs12710696(C;C)
Make rs12710696(C;T)
Make rs12710696(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position19121042
is asnp
is mentioned by
dbSNPrs12710696
ebirs12710696
HLIrs12710696
Exacrs12710696
Varsomers12710696
Maprs12710696
PheGenIrs12710696
hapmaprs12710696
1000 genomesrs12710696
hgdprs12710696
ensemblrs12710696
gopubmedrs12710696
geneviewrs12710696
scholarrs12710696
googlers12710696
pharmgkbrs12710696
gwascentralrs12710696
openSNPrs12710696
23andMers12710696
23andMe allrs12710696
SNP Nexus

SNPshotrs12710696
SNPdbers12710696
MSV3drs12710696
GWAS Ctlgrs12710696
GMAF0.3866
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23535733OA-icon.png]
Trait Breast cancer
Title Genome-wide association studies identify four ER negative-specific breast cancer risk loci.
Risk Allele
P-val 5E-8
Odds Ratio 1.10 [1.06-1.13]