rs688034
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | normal |
(C;T) | 1.1 | 1.1x risk higher risk for coronary artery disease |
(T;T) | 2 | 1.6x risk |
Reference | GRCh38 38.1/141 |
Chromosome | 22 |
Position | 26293669 |
Gene | SEZ6L |
is a | snp |
is | mentioned by |
dbSNP | rs688034 |
dbSNP (classic) | rs688034 |
ClinGen | rs688034 |
ebi | rs688034 |
HLI | rs688034 |
Exac | rs688034 |
Gnomad | rs688034 |
Varsome | rs688034 |
LitVar | rs688034 |
Map | rs688034 |
PheGenI | rs688034 |
Biobank | rs688034 |
1000 genomes | rs688034 |
hgdp | rs688034 |
ensembl | rs688034 |
geneview | rs688034 |
scholar | rs688034 |
rs688034 | |
pharmgkb | rs688034 |
gwascentral | rs688034 |
openSNP | rs688034 |
23andMe | rs688034 |
SNPshot | rs688034 |
SNPdbe | rs688034 |
MSV3d | rs688034 |
GWAS Ctlg | rs688034 |
GMAF | 0.1602 |
Max Magnitude | 2 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
rs688034 has been reported in a large study to be associated with heart disease, in particular, coronary artery disease.
The risk allele (oriented to the dbSNP entry) is (T); the odds ratio associated with heterozygotes is 1.11 (CI 0.98-1.25), and for homozygotes, 1.62 (CI 1.34-1.95). [PMID 17554300]
GWAS | |
---|---|
SNP | rs688034 |
PubMedID | [PMID 17554300] |
Condition | Coronary disease |
Gene | NR |
Risk Allele | T |
pValue | 4.00E-006 |
OR | 1.11 |
95% CI | 0.99-1.25 |
[PMID 19956433] Genetics of coronary artery disease: focus on genome-wide association studies.
[PMID 20017983] Evaluation of population impact of candidate polymorphisms for coronary heart disease in the Framingham Heart Study Offspring Cohort.