rs66785829
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs66785829(A;A) |
| Make rs66785829(A;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 4 |
| Position | 113365051 |
| Gene | ANK2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs66785829 |
| dbSNP (classic) | rs66785829 |
| ClinGen | rs66785829 |
| ebi | rs66785829 |
| HLI | rs66785829 |
| Exac | rs66785829 |
| Gnomad | rs66785829 |
| Varsome | rs66785829 |
| LitVar | rs66785829 |
| Map | rs66785829 |
| PheGenI | rs66785829 |
| Biobank | rs66785829 |
| 1000 genomes | rs66785829 |
| hgdp | rs66785829 |
| ensembl | rs66785829 |
| geneview | rs66785829 |
| scholar | rs66785829 |
| rs66785829 | |
| pharmgkb | rs66785829 |
| gwascentral | rs66785829 |
| openSNP | rs66785829 |
| 23andMe | rs66785829 |
| SNPshot | rs66785829 |
| SNPdbe | rs66785829 |
| MSV3d | rs66785829 |
| GWAS Ctlg | rs66785829 |
| Merged from | Rs66785830 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs66785829(A;A) rs66785829(C;C) |
| Alt | rs66785829(A;A) rs66785829(C;C) |
| Reference | Rs66785829(T;T) |
| Significance | Probable-non-pathogenic |
| Disease | Arrhythmia Long QT syndrome Cardiac arrhythmia not specified |
| Variation | info |
| Gene | ANK2 |
| CLNDBN | Arrhythmia Long QT syndrome Cardiac arrhythmia not specified |
| Reversed | 0 |
| HGVS | NC_000004.11:g.114286207T>A |
| CLNSRC | Cardiovascular Biomedical Research Unit ClinVar GeneDx |
| CLNACC | RCV000058344.3, RCV000168225.3, RCV000171748.3, RCV000211889.1, |
