rs6080699
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs6080699(C;C) |
| Make rs6080699(C;G) |
| Make rs6080699(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 20 |
| Position | 17453641 |
| Gene | PCSK2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6080699 |
| dbSNP (classic) | rs6080699 |
| ClinGen | rs6080699 |
| ebi | rs6080699 |
| HLI | rs6080699 |
| Exac | rs6080699 |
| Gnomad | rs6080699 |
| Varsome | rs6080699 |
| LitVar | rs6080699 |
| Map | rs6080699 |
| PheGenI | rs6080699 |
| Biobank | rs6080699 |
| 1000 genomes | rs6080699 |
| hgdp | rs6080699 |
| ensembl | rs6080699 |
| geneview | rs6080699 |
| scholar | rs6080699 |
| rs6080699 | |
| pharmgkb | rs6080699 |
| gwascentral | rs6080699 |
| openSNP | rs6080699 |
| 23andMe | rs6080699 |
| SNPshot | rs6080699 |
| SNPdbe | rs6080699 |
| MSV3d | rs6080699 |
| GWAS Ctlg | rs6080699 |
| GMAF | 0.2493 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 20036365] Association of genetic variants in SEMA3F, CLEC16A, LAMA3, and PCSK2 with myocardial infarction in Japanese individuals
