rs4304924
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4304924(A;A) |
Make rs4304924(A;G) |
Make rs4304924(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 13 |
Position | 78664790 |
is a | snp |
is | mentioned by |
dbSNP | rs4304924 |
dbSNP (classic) | rs4304924 |
ClinGen | rs4304924 |
ebi | rs4304924 |
HLI | rs4304924 |
Exac | rs4304924 |
Gnomad | rs4304924 |
Varsome | rs4304924 |
LitVar | rs4304924 |
Map | rs4304924 |
PheGenI | rs4304924 |
Biobank | rs4304924 |
1000 genomes | rs4304924 |
hgdp | rs4304924 |
ensembl | rs4304924 |
geneview | rs4304924 |
scholar | rs4304924 |
rs4304924 | |
pharmgkb | rs4304924 |
gwascentral | rs4304924 |
openSNP | rs4304924 |
23andMe | rs4304924 |
SNPshot | rs4304924 |
SNPdbe | rs4304924 |
MSV3d | rs4304924 |
GWAS Ctlg | rs4304924 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 24262325![]() |
Trait | Large artery stroke |
Title | Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants. |
Risk Allele | G |
P-val | 5E-6 |
Odds Ratio | 1.18 [1.1-1.27] |