RS121918282 SCN3B

Health Risk Chr 11:123653772 snv missense variant
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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
Population Frequencies
gnomAD ALL
100%
Other Variants in SCN3B
rs587777557 rs587777558 rs186341159 rs770801747 rs147205617 rs779277447 rs771342044 rs996152549 rs368054375 rs375755770
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