Progressive Myoclonic Epilepsy Type 3

Neurological 51 variants 2 genes

Upload your DNA to see your personal risk score for Progressive Myoclonic Epilepsy Type 3.

Associated Genes (2)

KCTD7 CLN3

Associated Variants (51)

RSID	Gene	Risk Allele	Odds Ratio	Evidence
RS1273966098	KCTD7	—	—	exploratory
RS2116774137	KCTD7	—	—	strong
RS1554397834	KCTD7	—	—	strong
RS368001837	KCTD7	—	—	strong
RS765235486	KCTD7	—	—	strong
RS747676224	KCTD7	—	—	strong
RS200575329	KCTD7	—	—	strong
RS1786631768	KCTD7	—	—	strong
RS769991459	KCTD7	—	—	strong
RS867319899	KCTD7	—	—	strong
RS2116773782	KCTD7	—	—	strong
RS2116775490	KCTD7	—	—	strong
RS2116775509	KCTD7	—	—	strong
RS1554397774	KCTD7	—	—	strong
RS2116763829	KCTD7	—	—	strong
RS2116755694	KCTD7	—	—	strong
RS141191660	KCTD7	—	—	strong
RS1207922864	KCTD7	—	—	strong
RS984651812	KCTD7	—	—	strong
RS367608044	KCTD7	—	—	strong
RS1440055692	KCTD7	—	—	strong
RS2535241170	KCTD7	—	—	strong
RS2535241375	KCTD7	—	—	strong
RS2535233194	KCTD7	—	—	strong
RS2535251918	KCTD7	—	—	strong
RS139585796	KCTD7	—	—	strong
RS387907246	KCTD7	—	—	strong
RS727502785	KCTD7	—	—	strong
RS387907260	KCTD7	—	—	strong
RS387907261	KCTD7	—	—	strong
RS387907262	KCTD7	—	—	strong
RS387907263	KCTD7	—	—	strong
RS587780370	KCTD7	—	—	strong
RS372150992	KCTD7	—	—	strong
RS145238250	KCTD7	—	—	strong
RS201296399	KCTD7	—	—	strong
RS200415747	KCTD7	—	—	strong
RS149255570	KCTD7	—	—	strong
RS267607199	KCTD7	—	—	strong
RS774026720	KCTD7	—	—	strong
RS199624315	KCTD7	—	—	strong
RS767984903	KCTD7	—	—	strong
RS796052686	KCTD7	—	—	strong
RS796052689	KCTD7	—	—	strong
RS137906617	CLN3	—	—	strong
RS753658170	KCTD7	—	—	strong
RS140932942	KCTD7	—	—	strong
RS750811871	KCTD7	—	—	strong
RS769023482	KCTD7	—	—	strong
RS376944331	KCTD7	—	—	strong

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