RS371067379 CHRNA2

Health Risk Chr 8:27467248
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Associated Conditions
Autosomal dominant nocturnal frontal lobe epilepsy 4
Inborn genetic diseases
Autosomal dominant nocturnal frontal lobe epilepsy 4
Inborn genetic diseases
Other Variants in CHRNA2
rs104894063 rs141721605 rs56344740 rs76140563 rs148009259 rs757567429 rs199810678 rs138682847 rs769608818 rs145238683
Ask Dr. Hemsworth about this variant