rs11708189
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11708189(A;A) |
Make rs11708189(A;G) |
Make rs11708189(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 140456518 |
Gene | CLSTN2, LOC105374132 |
is a | snp |
is | mentioned by |
dbSNP | rs11708189 |
dbSNP (classic) | rs11708189 |
ClinGen | rs11708189 |
ebi | rs11708189 |
HLI | rs11708189 |
Exac | rs11708189 |
Gnomad | rs11708189 |
Varsome | rs11708189 |
LitVar | rs11708189 |
Map | rs11708189 |
PheGenI | rs11708189 |
Biobank | rs11708189 |
1000 genomes | rs11708189 |
hgdp | rs11708189 |
ensembl | rs11708189 |
geneview | rs11708189 |
scholar | rs11708189 |
rs11708189 | |
pharmgkb | rs11708189 |
gwascentral | rs11708189 |
openSNP | rs11708189 |
23andMe | rs11708189 |
SNPshot | rs11708189 |
SNPdbe | rs11708189 |
MSV3d | rs11708189 |
GWAS Ctlg | rs11708189 |
GMAF | 0.4651 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21658281![]() |
Trait | |
Title | GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. |
Risk Allele | |
P-val | 0.000002 |
Odds Ratio | 1.1200 [1.07-1.18] |