RS7626962 SCN5A
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What This Variant Does
"rs7626962, also known as Ser1103Tyr or S1103Y, is a SNP in the cardiac sodium channel SCN5A gene. Al...
Associated Conditions
SUDDEN INFANT DEATH SYNDROME
Long QT syndrome 3
acquired
susceptibility to
Progressive familial heart block
type 1A
Ventricular fibrillation
paroxysmal familial
type 1
Sick sinus syndrome 1
Brugada syndrome
Dilated cardiomyopathy 1E
Cardiovascular phenotype
Brugada syndrome 1
Cardiac arrhythmia
Other Variants in SCN5A