RS121918282 SCN3B
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What This Variant Does
"[OMIM:?]
Associated Conditions
Brugada syndrome 7
Brugada syndrome
Atrial fibrillation
familial
16
Cardiovascular phenotype
Brugada syndrome 7
Brugada syndrome
Atrial fibrillation
familial
16
Cardiovascular phenotype
Other Variants in SCN3B