rs17228212
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 2 | >1.26x increased risk for heart disease |
| (C;T) | 2 | 1.26x increased risk for heart disease |
| (T;T) | 0 | normal |
| Reference | GRCh38 38.1/141 |
| Chromosome | 15 |
| Position | 67166301 |
| Gene | SMAD3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17228212 |
| dbSNP (classic) | rs17228212 |
| ClinGen | rs17228212 |
| ebi | rs17228212 |
| HLI | rs17228212 |
| Exac | rs17228212 |
| Gnomad | rs17228212 |
| Varsome | rs17228212 |
| LitVar | rs17228212 |
| Map | rs17228212 |
| PheGenI | rs17228212 |
| Biobank | rs17228212 |
| 1000 genomes | rs17228212 |
| hgdp | rs17228212 |
| ensembl | rs17228212 |
| geneview | rs17228212 |
| scholar | rs17228212 |
| rs17228212 | |
| pharmgkb | rs17228212 |
| gwascentral | rs17228212 |
| openSNP | rs17228212 |
| 23andMe | rs17228212 |
| SNPshot | rs17228212 |
| SNPdbe | rs17228212 |
| MSV3d | rs17228212 |
| GWAS Ctlg | rs17228212 |
| GMAF | 0.1561 |
| Max Magnitude | 2 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
rs17228212 is a SNP found to be associated with heart disease by the German MI (Myocardial infarction) Family Study group in two populations. The odds ratio per allele is 1.26 (CI: 1.11-1.44, p=0.0178).[PMID 17634449
]
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