rs11710077
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in complete genomics |
| Make rs11710077(A;T) |
| Make rs11710077(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 38616408 |
| Gene | SCN5A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11710077 |
| dbSNP (classic) | rs11710077 |
| ClinGen | rs11710077 |
| ebi | rs11710077 |
| HLI | rs11710077 |
| Exac | rs11710077 |
| Gnomad | rs11710077 |
| Varsome | rs11710077 |
| LitVar | rs11710077 |
| Map | rs11710077 |
| PheGenI | rs11710077 |
| Biobank | rs11710077 |
| 1000 genomes | rs11710077 |
| hgdp | rs11710077 |
| ensembl | rs11710077 |
| geneview | rs11710077 |
| scholar | rs11710077 |
| rs11710077 | |
| pharmgkb | rs11710077 |
| gwascentral | rs11710077 |
| openSNP | rs11710077 |
| 23andMe | rs11710077 |
| SNPshot | rs11710077 |
| SNPdbe | rs11710077 |
| MSV3d | rs11710077 |
| GWAS Ctlg | rs11710077 |
| GMAF | 0.1313 |
| Max Magnitude | 0 |
| ? | (A;A) (A;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21076409 ]
|
| Trait | |
| Title | Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction |
| Risk Allele | T |
| P-val | 0.000001 |
| Odds Ratio | 0.4400 [NR] ms decrease |
