rs6764363
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6764363(C;C) |
Make rs6764363(C;T) |
Make rs6764363(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 270666 |
Gene | CHL1 |
is a | snp |
is | mentioned by |
dbSNP | rs6764363 |
dbSNP (classic) | rs6764363 |
ClinGen | rs6764363 |
ebi | rs6764363 |
HLI | rs6764363 |
Exac | rs6764363 |
Gnomad | rs6764363 |
Varsome | rs6764363 |
LitVar | rs6764363 |
Map | rs6764363 |
PheGenI | rs6764363 |
Biobank | rs6764363 |
1000 genomes | rs6764363 |
hgdp | rs6764363 |
ensembl | rs6764363 |
geneview | rs6764363 |
scholar | rs6764363 |
rs6764363 | |
pharmgkb | rs6764363 |
gwascentral | rs6764363 |
openSNP | rs6764363 |
23andMe | rs6764363 |
SNPshot | rs6764363 |
SNPdbe | rs6764363 |
MSV3d | rs6764363 |
GWAS Ctlg | rs6764363 |
GMAF | 0.2851 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 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 | 0.000006 |
Odds Ratio | 1.1900 [1.10-1.28] |