rs11129795
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs11129795(A;A) |
| Make rs11129795(A;G) |
| Make rs11129795(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 38547672 |
| Gene | SCN5A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11129795 |
| dbSNP (classic) | rs11129795 |
| ClinGen | rs11129795 |
| ebi | rs11129795 |
| HLI | rs11129795 |
| Exac | rs11129795 |
| Gnomad | rs11129795 |
| Varsome | rs11129795 |
| LitVar | rs11129795 |
| Map | rs11129795 |
| PheGenI | rs11129795 |
| Biobank | rs11129795 |
| 1000 genomes | rs11129795 |
| hgdp | rs11129795 |
| ensembl | rs11129795 |
| geneview | rs11129795 |
| scholar | rs11129795 |
| rs11129795 | |
| pharmgkb | rs11129795 |
| gwascentral | rs11129795 |
| openSNP | rs11129795 |
| 23andMe | rs11129795 |
| SNPshot | rs11129795 |
| SNPdbe | rs11129795 |
| MSV3d | rs11129795 |
| GWAS Ctlg | rs11129795 |
| GMAF | 0.2062 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 19305409 ]
|
| Trait | QT interval |
| Title | Common variants at ten loci modulate the QT interval duration in the QTSCD Study |
| Risk Allele | A |
| P-val | 5E-14 |
| Odds Ratio | 1.27 [0.82-1.72] ms decrease |
| GWAS snp | |
|---|---|
| PMID | [PMID 20062063] |
| Trait | Electrocardiographic traits |
| Title | Several common variants modulate heart rate, PR interval and QRS duration |
| Risk Allele | G |
| P-val | 5E-10 |
| Odds Ratio | 8.24 [5.64-10.83] % SD decrease |
[PMID 20062060] Genome-wide association study of PR interval.
