rs11848785
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs11848785(A;A) |
| Make rs11848785(A;G) |
| Make rs11848785(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 14 |
| Position | 71590638 |
| Gene | SIPA1L1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11848785 |
| dbSNP (classic) | rs11848785 |
| ClinGen | rs11848785 |
| ebi | rs11848785 |
| HLI | rs11848785 |
| Exac | rs11848785 |
| Gnomad | rs11848785 |
| Varsome | rs11848785 |
| LitVar | rs11848785 |
| Map | rs11848785 |
| PheGenI | rs11848785 |
| Biobank | rs11848785 |
| 1000 genomes | rs11848785 |
| hgdp | rs11848785 |
| ensembl | rs11848785 |
| geneview | rs11848785 |
| scholar | rs11848785 |
| rs11848785 | |
| pharmgkb | rs11848785 |
| gwascentral | rs11848785 |
| openSNP | rs11848785 |
| 23andMe | rs11848785 |
| SNPshot | rs11848785 |
| SNPdbe | rs11848785 |
| MSV3d | rs11848785 |
| GWAS Ctlg | rs11848785 |
| GMAF | 0.1556 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21076409 ]
|
| Trait | |
| Title | Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction |
| Risk Allele | G |
| P-val | 1E-10 |
| Odds Ratio | 0.5000 [0.34-0.66] ms decrease |
[PMID 24922963] 163 Genetic Modifiers in Carriers of the SCN5A E1784K Mutation with Variable Phenotypic Expression - Long QT3 / Brugada Syndrome Overlap Disease
