RS1064795580 CHRNA2

Health Risk Chr 8:27467245
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Associated Conditions
Autosomal dominant nocturnal frontal lobe epilepsy
Inborn genetic diseases
Autosomal dominant nocturnal frontal lobe epilepsy
Inborn genetic diseases
Other Variants in CHRNA2
rs104894063 rs141721605 rs56344740 rs76140563 rs148009259 rs757567429 rs199810678 rs138682847 rs769608818 rs145238683
Ask Dr. Hemsworth about this variant