RS72544145 SCN2B

Health Risk Chr 11:118168739
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What This Variant Does
"CLNSIG=5
Associated Conditions
Atrial fibrillation
familial
14
Cardiovascular phenotype
Atrial fibrillation
familial
14
Cardiovascular phenotype
Other Variants in SCN2B
rs17121819 rs144248214 rs17121818 rs115353159 rs1064796044 rs200264107 rs774866184 rs765743471 rs758238682 rs367981116
Ask Dr. Hemsworth about this variant