RS281865067 CHRNA4

Health Risk Chr 20:63350538
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What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal dominant nocturnal frontal lobe epilepsy 1
Autosomal dominant nocturnal frontal lobe epilepsy 1
Other Variants in CHRNA4
rs121909580 rs28931591 rs121912267 rs121912268 rs121912274 rs121912277 rs121912278 rs121912280 rs121912281 rs121912282
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