rs7192724
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7192724(C;C) |
Make rs7192724(C;G) |
Make rs7192724(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 81924693 |
Gene | PLCG2 |
is a | snp |
is | mentioned by |
dbSNP | rs7192724 |
dbSNP (classic) | rs7192724 |
ClinGen | rs7192724 |
ebi | rs7192724 |
HLI | rs7192724 |
Exac | rs7192724 |
Gnomad | rs7192724 |
Varsome | rs7192724 |
LitVar | rs7192724 |
Map | rs7192724 |
PheGenI | rs7192724 |
Biobank | rs7192724 |
1000 genomes | rs7192724 |
hgdp | rs7192724 |
ensembl | rs7192724 |
geneview | rs7192724 |
scholar | rs7192724 |
rs7192724 | |
pharmgkb | rs7192724 |
gwascentral | rs7192724 |
openSNP | rs7192724 |
23andMe | rs7192724 |
SNPshot | rs7192724 |
SNPdbe | rs7192724 |
MSV3d | rs7192724 |
GWAS Ctlg | rs7192724 |
Max Magnitude | 0 |
? | (C;C) (C;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 | 3E-6 |
Odds Ratio | 1.24 [1.13-1.36] |