rs9579199
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs9579199(A;A) |
Make rs9579199(A;G) |
Make rs9579199(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 13 |
Position | 28590646 |
is a | snp |
is | mentioned by |
dbSNP | rs9579199 |
dbSNP (classic) | rs9579199 |
ClinGen | rs9579199 |
ebi | rs9579199 |
HLI | rs9579199 |
Exac | rs9579199 |
Gnomad | rs9579199 |
Varsome | rs9579199 |
LitVar | rs9579199 |
Map | rs9579199 |
PheGenI | rs9579199 |
Biobank | rs9579199 |
1000 genomes | rs9579199 |
hgdp | rs9579199 |
ensembl | rs9579199 |
geneview | rs9579199 |
scholar | rs9579199 |
rs9579199 | |
pharmgkb | rs9579199 |
gwascentral | rs9579199 |
openSNP | rs9579199 |
23andMe | rs9579199 |
SNPshot | rs9579199 |
SNPdbe | rs9579199 |
MSV3d | rs9579199 |
GWAS Ctlg | rs9579199 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 24080446] |
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] |