rs2549513
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2549513(A;A) |
| Make rs2549513(A;C) |
| Make rs2549513(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 16 |
| Position | 79516830 |
| Gene | MAF |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2549513 |
| dbSNP (classic) | rs2549513 |
| ClinGen | rs2549513 |
| ebi | rs2549513 |
| HLI | rs2549513 |
| Exac | rs2549513 |
| Gnomad | rs2549513 |
| Varsome | rs2549513 |
| LitVar | rs2549513 |
| Map | rs2549513 |
| PheGenI | rs2549513 |
| Biobank | rs2549513 |
| 1000 genomes | rs2549513 |
| hgdp | rs2549513 |
| ensembl | rs2549513 |
| geneview | rs2549513 |
| scholar | rs2549513 |
| rs2549513 | |
| pharmgkb | rs2549513 |
| gwascentral | rs2549513 |
| openSNP | rs2549513 |
| 23andMe | rs2549513 |
| SNPshot | rs2549513 |
| SNPdbe | rs2549513 |
| MSV3d | rs2549513 |
| GWAS Ctlg | rs2549513 |
| GMAF | 0.1529 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
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| ||
[PMID 22856164] [Evaluation of association between 9 genetic polymorphism and myocardial infarction in the Siberian population]
[PMID 17903304
] Framingham Heart Study 100K project: genome-wide associations for cardiovascular disease outcomes.
[PMID 20017983] Evaluation of population impact of candidate polymorphisms for coronary heart disease in the Framingham Heart Study Offspring Cohort.
[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]
