RS121912243 CHRNA4

Health Risk Chr 20:63350968 snv missense variant
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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
Population Frequencies
gnomAD ALL
0%
1kG AFR
100%
1kG ALL
100%
1kG AMR
100%
1kG EAS
100%
1kG EUR
0.1%
1kG SAS
100%
Other Variants in CHRNA4
rs121909580 rs28931591 rs281865067 rs121912267 rs121912268 rs121912274 rs121912277 rs121912278 rs121912280 rs121912281
Ask Dr. Hemsworth about this variant