RS74315291 CHRNB2

Health Risk Chr 1:154571682
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What This Variant Does
"[OMIM:?]
Associated Conditions
Autosomal dominant nocturnal frontal lobe epilepsy 3
Autosomal dominant nocturnal frontal lobe epilepsy 3
Autosomal dominant nocturnal frontal lobe epilepsy
Inborn genetic diseases
Autosomal dominant nocturnal frontal lobe epilepsy 1
Autosomal dominant nocturnal frontal lobe epilepsy 3
Autosomal dominant nocturnal frontal lobe epilepsy
Autosomal dominant nocturnal frontal lobe epilepsy 3
Autosomal dominant nocturnal frontal lobe epilepsy 3
Autosomal dominant nocturnal frontal lobe epilepsy
Inborn genetic diseases
Autosomal dominant nocturnal frontal lobe epilepsy 1
Autosomal dominant nocturnal frontal lobe epilepsy 3
Autosomal dominant nocturnal frontal lobe epilepsy
Other Variants in CHRNB2
rs281865070 rs144813907 rs55685423 rs141735618 rs199885651 rs796052329 rs780175030 rs753731408 rs770055798 rs190374968
Ask Dr. Hemsworth about this variant