rs2123536
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs2123536(A;A) |
Make rs2123536(A;G) |
Make rs2123536(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 19745816 |
is a | snp |
is | mentioned by |
dbSNP | rs2123536 |
dbSNP (classic) | rs2123536 |
ClinGen | rs2123536 |
ebi | rs2123536 |
HLI | rs2123536 |
Exac | rs2123536 |
Gnomad | rs2123536 |
Varsome | rs2123536 |
LitVar | rs2123536 |
Map | rs2123536 |
PheGenI | rs2123536 |
Biobank | rs2123536 |
1000 genomes | rs2123536 |
hgdp | rs2123536 |
ensembl | rs2123536 |
geneview | rs2123536 |
scholar | rs2123536 |
rs2123536 | |
pharmgkb | rs2123536 |
gwascentral | rs2123536 |
openSNP | rs2123536 |
23andMe | rs2123536 |
SNPshot | rs2123536 |
SNPdbe | rs2123536 |
MSV3d | rs2123536 |
GWAS Ctlg | rs2123536 |
GMAF | 0.2268 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 22751097] |
Trait | Coronary heart disease |
Title | Genome-wide association study in Han Chinese identifies four new susceptibility loci for coronary artery disease. |
Risk Allele | T |
P-val | 7E-11 |
Odds Ratio | 1.12 [1.08-1.16] |