rs11708996
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common on affy axiom data |
| Make rs11708996(C;C) |
| Make rs11708996(C;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 38592432 |
| Gene | SCN5A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11708996 |
| dbSNP (classic) | rs11708996 |
| ClinGen | rs11708996 |
| ebi | rs11708996 |
| HLI | rs11708996 |
| Exac | rs11708996 |
| Gnomad | rs11708996 |
| Varsome | rs11708996 |
| LitVar | rs11708996 |
| Map | rs11708996 |
| PheGenI | rs11708996 |
| Biobank | rs11708996 |
| 1000 genomes | rs11708996 |
| hgdp | rs11708996 |
| ensembl | rs11708996 |
| geneview | rs11708996 |
| scholar | rs11708996 |
| rs11708996 | |
| pharmgkb | rs11708996 |
| gwascentral | rs11708996 |
| openSNP | rs11708996 |
| 23andMe | rs11708996 |
| SNPshot | rs11708996 |
| SNPdbe | rs11708996 |
| MSV3d | rs11708996 |
| GWAS Ctlg | rs11708996 |
| GMAF | 0.08999 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20062060 ]
|
| Trait | PR interval |
| Title | Genome-wide association study of PR interval. |
| Risk Allele | C |
| P-val | 6E-26 |
| Odds Ratio | 3.04 [2.47-3.61] ms increase |
| GWAS snp | |
|---|---|
| PMID | [PMID 21076409]
|
| Trait | |
| Title | Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction |
| Risk Allele | C |
| P-val | 0.000007 |
| Odds Ratio | 0.4700 [NR] ms increase |
[PMID 21347284] Genome-wide association studies of the PR interval in African Americans.
| GWAS snp | |
|---|---|
| PMID | [PMID 23872634]
|
| Trait | Brugada syndrome |
| Title | Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death. |
| Risk Allele | C |
| P-val | 1E-14 |
| Odds Ratio | 1.73 [1.51-1.99] |
