rs1014922
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs1014922(A;A) |
Make rs1014922(A;C) |
Make rs1014922(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 15 |
Position | 94622351 |
is a | snp |
is | mentioned by |
dbSNP | rs1014922 |
dbSNP (classic) | rs1014922 |
ClinGen | rs1014922 |
ebi | rs1014922 |
HLI | rs1014922 |
Exac | rs1014922 |
Gnomad | rs1014922 |
Varsome | rs1014922 |
LitVar | rs1014922 |
Map | rs1014922 |
PheGenI | rs1014922 |
Biobank | rs1014922 |
1000 genomes | rs1014922 |
hgdp | rs1014922 |
ensembl | rs1014922 |
geneview | rs1014922 |
scholar | rs1014922 |
rs1014922 | |
pharmgkb | rs1014922 |
gwascentral | rs1014922 |
openSNP | rs1014922 |
23andMe | rs1014922 |
SNPshot | rs1014922 |
SNPdbe | rs1014922 |
MSV3d | rs1014922 |
GWAS Ctlg | rs1014922 |
GMAF | 0.1933 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 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 | 0.000003 |
Odds Ratio | 1.3600 [1.20-1.55] |