Autosomal Dominant Nocturnal Frontal Lobe Epilepsy 5

Neurological 193 variants 2 genes

Upload your DNA to see your personal risk score for Autosomal Dominant Nocturnal Frontal Lobe Epilepsy 5.

Associated Genes (2)

KCNT1 SPAG1

Associated Variants (193)

RSID	Gene	Risk Allele	Odds Ratio	Evidence
RS886043455	KCNT1	—	—	strong
RS772892562	KCNT1	—	—	strong
RS752032951	KCNT1	—	—	strong
RS149927148	KCNT1	—	—	strong
RS370046449	KCNT1	—	—	strong
RS554828530	KCNT1	—	—	strong
RS370085077	KCNT1	—	—	strong
RS138282349	KCNT1	—	—	strong
RS151272083	KCNT1	—	—	strong
RS869312682	KCNT1	—	—	strong
RS147551342	KCNT1	—	—	strong
RS866242631	KCNT1	—	—	strong
RS886041691	KCNT1	—	—	strong
RS143678590	KCNT1	—	—	strong
RS752453368	KCNT1	—	—	strong
RS558966732	KCNT1	—	—	strong
RS796214553	KCNT1	—	—	strong
RS761045901	KCNT1	—	—	strong
RS1057518066	KCNT1	—	—	strong
RS758152252	KCNT1	—	—	strong
RS372998864	KCNT1	—	—	strong
RS780875110	KCNT1	—	—	strong
RS769406687	KCNT1	—	—	strong
RS779590747	KCNT1	—	—	strong
RS2491046098	KCNT1	—	—	strong
RS369983077	KCNT1	—	—	strong
RS397515403	KCNT1	—	—	strong
RS397515404	KCNT1	—	—	strong
RS397515405	KCNT1	—	—	strong
RS397515406	KCNT1	—	—	strong
RS397515407	KCNT1	—	—	strong
RS397518459	SPAG1	—	—	strong
RS201740530	SPAG1	—	—	strong
RS886037653	SPAG1	—	—	strong
RS886044717	KCNT1	—	—	strong
RS587777264	KCNT1	—	—	strong
RS547714141	KCNT1	—	—	strong
RS143355299	KCNT1	—	—	strong
RS397515402	KCNT1	—	—	strong
RS200694691	KCNT1	—	—	strong
RS797044544	KCNT1	—	—	strong
RS146152956	KCNT1	—	—	strong
RS144766991	KCNT1	—	—	strong
RS146070496	KCNT1	—	—	strong
RS142756900	KCNT1	—	—	strong
RS539139475	KCNT1	—	—	strong
RS147306623	KCNT1	—	—	strong
RS371135108	KCNT1	—	—	strong
RS532620254	KCNT1	—	—	strong
RS376314779	KCNT1	—	—	strong

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