RS267607028 SCN1B

Health Risk Chr 19:35033827
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Brugada syndrome 5
Atrial fibrillation
familial
13
Brugada syndrome 5
Atrial fibrillation
familial
13
Other Variants in SCN1B
rs104894718 rs724159982 rs267607029 rs193922728 rs16969925 rs587781152 rs72558026 rs72552027 rs786205834 rs786205837
Ask Dr. Hemsworth about this variant