Geno
|
Mag
|
Summary
|
(T;T)
|
0
|
common in clinvar
|
[PMID 17534376] Confirmation of associations between ion channel gene SNPs and QTc interval duration in healthy subjects.
[PMID 18368697] SCN5A variants in Japanese patients with left ventricular noncompaction and arrhythmia.
ClinVar
|
Risk
|
rs1805126(C;C) |
Alt
|
rs1805126(C;C) |
Reference
|
Rs1805126(T;T) |
Significance |
Probable-non-pathogenic |
Disease |
not specified Cardiovascular phenotype Brugada syndrome Romano-Ward syndrome Long QT syndrome Dilated Cardiomyopathy Paroxysmal familial ventricular fibrillation Sick sinus syndrome Progressive familial heart block |
Variation | info |
---|
Gene |
SCN5A |
CLNDBN |
not specified Cardiovascular phenotype Brugada syndrome Romano-Ward syndrome Long QT syndrome Dilated Cardiomyopathy, Dominant Paroxysmal familial ventricular fibrillation Sick sinus syndrome Progressive familial heart block |
Reversed |
1 |
HGVS |
NC_000003.11:g.38592406A>G |
CLNSRC |
ClinVar GeneDx |
CLNACC |
RCV000041627.5, RCV000243623.1, RCV000286827.1, RCV000302171.1, RCV000335948.1, RCV000341786.1, RCV000347752.1, RCV000371957.1, RCV000390614.1, |