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rs12422552

From SNPedia

Orientationplus
Stabilizedplus
Make rs12422552(C;C)
Make rs12422552(C;G)
Make rs12422552(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position14260997
is asnp
is mentioned by
dbSNPrs12422552
dbSNP (classic)rs12422552
ClinGenrs12422552
ebirs12422552
HLIrs12422552
Exacrs12422552
Gnomadrs12422552
Varsomers12422552
LitVarrs12422552
Maprs12422552
PheGenIrs12422552
Biobankrs12422552
1000 genomesrs12422552
hgdprs12422552
ensemblrs12422552
geneviewrs12422552
scholarrs12422552
googlers12422552
pharmgkbrs12422552
gwascentralrs12422552
openSNPrs12422552
23andMers12422552
SNPshotrs12422552
SNPdbers12422552
MSV3drs12422552
GWAS Ctlgrs12422552
GMAF0.2906
Max Magnitude0
? (C;C) (C;G) (G;G) 28


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 C
P-val 4E-8
Odds Ratio 1.05 [1.03-1.07]