RS144813907 CHRNB2

Health Risk Chr 1:154575908
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Associated Conditions
Autosomal dominant nocturnal frontal lobe epilepsy
Inborn genetic diseases
CHRNB2-related disorder
Autosomal dominant nocturnal frontal lobe epilepsy
Inborn genetic diseases
CHRNB2-related disorder
Other Variants in CHRNB2
rs74315291 rs281865070 rs55685423 rs141735618 rs199885651 rs796052329 rs780175030 rs753731408 rs770055798 rs190374968
Ask Dr. Hemsworth about this variant