rs3807375
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs3807375(A;A) |
| Make rs3807375(A;G) |
| Make rs3807375(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 150970122 |
| Gene | KCNH2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3807375 |
| dbSNP (classic) | rs3807375 |
| ClinGen | rs3807375 |
| ebi | rs3807375 |
| HLI | rs3807375 |
| Exac | rs3807375 |
| Gnomad | rs3807375 |
| Varsome | rs3807375 |
| LitVar | rs3807375 |
| Map | rs3807375 |
| PheGenI | rs3807375 |
| Biobank | rs3807375 |
| 1000 genomes | rs3807375 |
| hgdp | rs3807375 |
| ensembl | rs3807375 |
| geneview | rs3807375 |
| scholar | rs3807375 |
| rs3807375 | |
| pharmgkb | rs3807375 |
| gwascentral | rs3807375 |
| openSNP | rs3807375 |
| 23andMe | rs3807375 |
| SNPshot | rs3807375 |
| SNPdbe | rs3807375 |
| MSV3d | rs3807375 |
| GWAS Ctlg | rs3807375 |
| GMAF | 0.4219 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 19019189
] QT interval rs3807375 rs2880058
| GWAS snp | |
|---|---|
| PMID | [PMID 20062063] |
| Trait | Electrocardiographic traits |
| Title | Several common variants modulate heart rate, PR interval and QRS duration |
| Risk Allele | T |
| P-val | 5E-11 |
| Odds Ratio | 11.95 [8.39-15.51] % SD increase |
[PMID 20215044] Relationship of Common Candidate Gene Variants to Electrocardiographic T-Wave Peak to T-Wave End Interval and T-Wave Morphology Parameters
[PMID 19214780] In silico investigations on functional and haplotype tag SNPs associated with congenital long QT syndromes (LQTSs).
[PMID 19305408] Common variants at ten loci influence QT interval duration in the QTGEN Study.
[PMID 19490382] Genetic polymorphism of KCNH2 confers predisposition of acquired atrial fibrillation in Chinese.
