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rs9579199

From SNPedia

Orientationplus
Stabilizedplus
Make rs9579199(A;A)
Make rs9579199(A;G)
Make rs9579199(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position28590646
is asnp
is mentioned by
dbSNPrs9579199
ebirs9579199
HLIrs9579199
Exacrs9579199
Varsomers9579199
Maprs9579199
PheGenIrs9579199
hapmaprs9579199
1000 genomesrs9579199
hgdprs9579199
ensemblrs9579199
gopubmedrs9579199
geneviewrs9579199
scholarrs9579199
googlers9579199
pharmgkbrs9579199
gwascentralrs9579199
openSNPrs9579199
23andMers9579199
23andMe allrs9579199
SNP Nexus

SNPshotrs9579199
SNPdbers9579199
MSV3drs9579199
GWAS Ctlgrs9579199
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 24080446OA-icon.png]
Trait Breast cancer (menopausal hormone therapy interaction)
Title Genetic modifiers of menopausal hormone replacement therapy and breast cancer risk: a genome-wide interaction study.
Risk Allele
P-val 8E-6
Odds Ratio 1.20 [1.11-1.32]