RS770055798 CHRNB2

Health Risk Chr 1:154571994
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Associated Conditions
Autosomal dominant nocturnal frontal lobe epilepsy
Inborn genetic diseases
Autosomal dominant nocturnal frontal lobe epilepsy
Inborn genetic diseases
Other Variants in CHRNB2
rs74315291 rs281865070 rs144813907 rs55685423 rs141735618 rs199885651 rs796052329 rs780175030 rs753731408 rs190374968
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