rs6666258
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs6666258(C;C) |
| Make rs6666258(C;G) |
| Make rs6666258(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 154841792 |
| Gene | KCNN3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6666258 |
| dbSNP (classic) | rs6666258 |
| ClinGen | rs6666258 |
| ebi | rs6666258 |
| HLI | rs6666258 |
| Exac | rs6666258 |
| Gnomad | rs6666258 |
| Varsome | rs6666258 |
| LitVar | rs6666258 |
| Map | rs6666258 |
| PheGenI | rs6666258 |
| Biobank | rs6666258 |
| 1000 genomes | rs6666258 |
| hgdp | rs6666258 |
| ensembl | rs6666258 |
| geneview | rs6666258 |
| scholar | rs6666258 |
| rs6666258 | |
| pharmgkb | rs6666258 |
| gwascentral | rs6666258 |
| openSNP | rs6666258 |
| 23andMe | rs6666258 |
| SNPshot | rs6666258 |
| SNPdbe | rs6666258 |
| MSV3d | rs6666258 |
| GWAS Ctlg | rs6666258 |
| GMAF | 0.2479 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22544366 ]
|
| Trait | |
| Title | Meta-analysis identifies six new susceptibility loci for atrial fibrillation. |
| Risk Allele | C |
| P-val | 2E-14 |
| Odds Ratio | 1.1800 None |
[PMID 27179719] Impact of genetic variants on the upstream efficacy of renin-angiotensin system inhibitors for the prevention of atrial fibrillation.
[PMID 29624624] Genetic modulation of atrial fibrillation risk in a Hispanic/Latino cohort.
