rs8055236
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | |
(G;G) | 1.7 | common, but 2.2x higher risk for heart disease |
(G;T) | 1.7 | 1.9x risk for heart disease |
(T;T) | 0 | normal |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 83178793 |
Gene | CDH13 |
is a | snp |
is | mentioned by |
dbSNP | rs8055236 |
dbSNP (classic) | rs8055236 |
ClinGen | rs8055236 |
ebi | rs8055236 |
HLI | rs8055236 |
Exac | rs8055236 |
Gnomad | rs8055236 |
Varsome | rs8055236 |
LitVar | rs8055236 |
Map | rs8055236 |
PheGenI | rs8055236 |
Biobank | rs8055236 |
1000 genomes | rs8055236 |
hgdp | rs8055236 |
ensembl | rs8055236 |
geneview | rs8055236 |
scholar | rs8055236 |
rs8055236 | |
pharmgkb | rs8055236 |
gwascentral | rs8055236 |
openSNP | rs8055236 |
23andMe | rs8055236 |
SNPshot | rs8055236 |
SNPdbe | rs8055236 |
MSV3d | rs8055236 |
GWAS Ctlg | rs8055236 |
GMAF | 0.2447 |
Max Magnitude | 1.7 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
rs8055236 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 (G); the odds ratio associated with heterozygotes is 1.91 (CI 1.33-2.74), and for homozygotes, 2.23 (CI 1.56-3.17). [PMID 17554300]
GWAS | |
---|---|
SNP | rs8055236 |
PubMedID | [PMID 17554300] |
Condition | Coronary disease |
Gene | NR |
Risk Allele | G |
pValue | 6.00E-006 |
OR | 1.91 |
95% CI | 1.33-2.74 |
[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.