RS199885651 CHRNB2

Health Risk Chr 1:154570331
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Associated Conditions
Microcephaly
Deeply set eye
Seizure
Autosomal dominant nocturnal frontal lobe epilepsy
Autosomal dominant nocturnal frontal lobe epilepsy 3
Inborn genetic diseases
Microcephaly
Deeply set eye
Seizure
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 rs796052329 rs780175030 rs753731408 rs770055798 rs190374968
Ask Dr. Hemsworth about this variant