RS281865070 CHRNB2

Health Risk Chr 1:154571746
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What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal dominant nocturnal frontal lobe epilepsy
Autosomal dominant nocturnal frontal lobe epilepsy
Other Variants in CHRNB2
rs74315291 rs144813907 rs55685423 rs141735618 rs199885651 rs796052329 rs780175030 rs753731408 rs770055798 rs190374968
Ask Dr. Hemsworth about this variant