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rs11199914

From SNPedia

Orientationplus
Stabilizedplus
Make rs11199914(C;C)
Make rs11199914(C;T)
Make rs11199914(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position121334387
is asnp
is mentioned by
dbSNPrs11199914
ebirs11199914
HLIrs11199914
Exacrs11199914
Varsomers11199914
Maprs11199914
PheGenIrs11199914
hapmaprs11199914
1000 genomesrs11199914
hgdprs11199914
ensemblrs11199914
gopubmedrs11199914
geneviewrs11199914
scholarrs11199914
googlers11199914
pharmgkbrs11199914
gwascentralrs11199914
openSNPrs11199914
23andMers11199914
23andMe allrs11199914
SNP Nexus

SNPshotrs11199914
SNPdbers11199914
MSV3drs11199914
GWAS Ctlgrs11199914
GMAF0.4027
Max Magnitude
? (C;C) (C;T) (T;T) 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 2E-8
Odds Ratio 1.05 [1.03-1.08]