RS797044544 KCNT1

Health Risk Chr 9:135778781
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What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal dominant nocturnal frontal lobe epilepsy 5
Autosomal dominant nocturnal frontal lobe epilepsy 5
Other Variants in KCNT1
rs397515402 rs397515403 rs397515404 rs370521183 rs397515405 rs397515406 rs397515407 rs886044717 rs587777264 rs547714141
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