rs499818
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs499818(A;A) |
| Make rs499818(A;G) |
| Make rs499818(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 13332235 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs499818 |
| dbSNP (classic) | rs499818 |
| ClinGen | rs499818 |
| ebi | rs499818 |
| HLI | rs499818 |
| Exac | rs499818 |
| Gnomad | rs499818 |
| Varsome | rs499818 |
| LitVar | rs499818 |
| Map | rs499818 |
| PheGenI | rs499818 |
| Biobank | rs499818 |
| 1000 genomes | rs499818 |
| hgdp | rs499818 |
| ensembl | rs499818 |
| geneview | rs499818 |
| scholar | rs499818 |
| rs499818 | |
| pharmgkb | rs499818 |
| gwascentral | rs499818 |
| openSNP | rs499818 |
| 23andMe | rs499818 |
| SNPshot | rs499818 |
| SNPdbe | rs499818 |
| MSV3d | rs499818 |
| GWAS Ctlg | rs499818 |
| GMAF | 0.1873 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS | |
|---|---|
| SNP | rs499818 |
| PubMedID | [PMID 17903304 ]
|
| Condition | Major CVD |
| Gene | Intergenic |
| Risk Allele | |
| pValue | 7.00E-006 |
| OR | NA |
| 95% CI | |
[PMID 22856164] [Evaluation of association between 9 genetic polymorphism and myocardial infarction in the Siberian population]
[PMID 20823317] is-rSNP: a novel technique for in silico regulatory SNP detection.
[PMID 22042884] Association of genetic variants and incident coronary heart disease in multiethnic cohorts: the PAGE study.
[PMID 24087953] [Genetic predictors of myocardial infarction in subjects of young age]
