RS796052329 CHRNB2

Health Risk Chr 1:154570361
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Associated Conditions
Autosomal dominant nocturnal frontal lobe epilepsy
Autosomal dominant nocturnal frontal lobe epilepsy 3
Inborn genetic diseases
Autosomal dominant nocturnal frontal lobe epilepsy
Autosomal dominant nocturnal frontal lobe epilepsy 3
Inborn genetic diseases
Other Variants in CHRNB2
rs74315291 rs281865070 rs144813907 rs55685423 rs141735618 rs199885651 rs780175030 rs753731408 rs770055798 rs190374968
Ask Dr. Hemsworth about this variant