RS121912243 CHRNA4

Health Risk Chr 20:63350969
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What This Variant Does
"CLNSIG=4
Associated Conditions
Tobacco use disorder
Inborn genetic diseases
Autosomal dominant nocturnal frontal lobe epilepsy
Amyotrophic lateral sclerosis
Tobacco use disorder
Inborn genetic diseases
Autosomal dominant nocturnal frontal lobe epilepsy
Amyotrophic lateral sclerosis
Other Variants in CHRNA4
rs121909580 rs28931591 rs281865067 rs121912267 rs121912268 rs121912274 rs121912277 rs121912278 rs121912280 rs121912281
Ask Dr. Hemsworth about this variant