rs9978223
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs9978223(A;A) |
| Make rs9978223(A;G) |
| Make rs9978223(G;G) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 21 |
| Position | 33398052 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9978223 |
| dbSNP (classic) | rs9978223 |
| ClinGen | rs9978223 |
| ebi | rs9978223 |
| HLI | rs9978223 |
| Exac | rs9978223 |
| Gnomad | rs9978223 |
| Varsome | rs9978223 |
| LitVar | rs9978223 |
| Map | rs9978223 |
| PheGenI | rs9978223 |
| Biobank | rs9978223 |
| 1000 genomes | rs9978223 |
| hgdp | rs9978223 |
| ensembl | rs9978223 |
| geneview | rs9978223 |
| scholar | rs9978223 |
| rs9978223 | |
| pharmgkb | rs9978223 |
| gwascentral | rs9978223 |
| openSNP | rs9978223 |
| 23andMe | rs9978223 |
| SNPshot | rs9978223 |
| SNPdbe | rs9978223 |
| MSV3d | rs9978223 |
| GWAS Ctlg | rs9978223 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 29434065
] Identification of a single nucleotide polymorphism indicative of high risk in acute myocardial infarction.
