RS28931591 CHRNA4

Health Risk Chr 20:63350560
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What This Variant Does
"[OMIM:EPILEPSY, NOCTURNAL FRONTAL LOBE, TYPE 1]
Associated Conditions
Autosomal dominant nocturnal frontal lobe epilepsy 1
Autosomal dominant nocturnal frontal lobe epilepsy
Inborn genetic diseases
Autosomal dominant nocturnal frontal lobe epilepsy 1
Autosomal dominant nocturnal frontal lobe epilepsy
Inborn genetic diseases
Other Variants in CHRNA4
rs121909580 rs281865067 rs121912267 rs121912268 rs121912274 rs121912277 rs121912278 rs121912280 rs121912281 rs121912282
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