Gene table: search width pubmed_id = 16684018


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Disease phenotype
Item
in
this
table
Key
references
Gene symbol (chromosome)

protein
All allelic disease phenotypes - locus/disease symbols
Atrial fibrillation, 10 - (AD)
10.167
16684018
SCN5A (3p22.2)
Voltage-gated sodium channel type V alpha
* Progressive familial heart block, type I - PFHBI
* Cardiomyopathy, dilated, 1E - CMD1E
* Sick Sinus Syndrome 1, autosomal recessive - SSS1
* Ventricular fibrillation, idiopathic - IVF
* Ventricular fibrillation, paroxysmal familial - VF
* Hereditary bundle branch system defect - HBBD
* Cardiac conduction defect, progressive - PCCD
* Brugada syndrome 1 - BRGDA1
* Atrial fibrillation, 10 - ATFB10
* Long QT syndrome-3 - LQT3