rs2269648
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 |
| Make rs2269648(C;T) |
| Make rs2269648(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 169586812 |
| Gene | F5 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2269648 |
| dbSNP (classic) | rs2269648 |
| ClinGen | rs2269648 |
| ebi | rs2269648 |
| HLI | rs2269648 |
| Exac | rs2269648 |
| Gnomad | rs2269648 |
| Varsome | rs2269648 |
| LitVar | rs2269648 |
| Map | rs2269648 |
| PheGenI | rs2269648 |
| Biobank | rs2269648 |
| 1000 genomes | rs2269648 |
| hgdp | rs2269648 |
| ensembl | rs2269648 |
| geneview | rs2269648 |
| scholar | rs2269648 |
| rs2269648 | |
| pharmgkb | rs2269648 |
| gwascentral | rs2269648 |
| openSNP | rs2269648 |
| 23andMe | rs2269648 |
| SNPshot | rs2269648 |
| SNPdbe | rs2269648 |
| MSV3d | rs2269648 |
| GWAS Ctlg | rs2269648 |
| GMAF | 0.3939 |
| Max Magnitude | 0 |
linked to Cardiovascular Events
Several CVD risk variants were identified: In women, the combination of F5 rs7542281 × THBD rs1042580, together with three single F5 SNPs, was associated with CVD events. Among men, PROC rs1041296, when combined with either ICAM1 rs5030341 or F5 rs2269648, was associated with total mortality. As a single variant, PROC rs1401296, together with the F5 Leiden mutation, was associated with ischemic stroke events.[PMID 17677000
]
[PMID 18974842] Gender differences in genetic risk profiles for cardiovascular disease.
[PMID 26054681] Association of seven thrombotic pathway gene CpG-SNPs with coronary heart disease
