Encephalopathy

Other 265 variants 13 genes

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Associated Genes (13)

SNORA31 TBK1 IRF3 SERAC1 CPT2 TBCE HMBS DNM1L ANKRD11;TRAPPC2L UNC80 ALG1 KCNE3;LIPT2 MECP2

Associated Variants (265)

RSID	Gene	Risk Allele	Odds Ratio	Evidence
RS768983518	SNORA31	—	—	exploratory
RS376154815	SNORA31	—	—	exploratory
RS577690999	SNORA31	—	—	exploratory
RS757938814	SNORA31	—	—	exploratory
RS1555203557	TBK1	—	—	exploratory
RS1555202947	TBK1	—	—	exploratory
RS750526659	IRF3	—	—	exploratory
RS147085187	SERAC1	—	—	strong
RS727503887	CPT2	—	—	strong
RS200022583	TBCE	—	—	strong
RS794727616	CPT2	—	—	strong
RS201065226	CPT2	—	—	strong
RS368311455	CPT2	—	—	strong
RS373714948	CPT2	—	—	strong
RS797045105	SERAC1	—	—	strong
RS768913919	SERAC1	—	—	strong
RS767780913	SERAC1	—	—	strong
RS780275814	SERAC1	—	—	strong
RS199632531	SERAC1	—	—	strong
RS150763621	HMBS	—	—	strong
RS863223953	DNM1L	—	—	strong
RS138133550	DNM1L	—	—	strong
RS863225296	ANKRD11;TRAPPC2L	—	—	strong
RS864321623	UNC80	—	—	strong
RS759086398	CPT2	—	—	strong
RS74315296	CPT2	—	—	strong
RS118204101	HMBS	—	—	strong
RS118204109	HMBS	—	—	strong
RS118204119	HMBS	—	—	strong
RS28939378	ALG1	—	—	strong
RS767004810	TBCE	—	—	strong
RS17215437	KCNE3;LIPT2	—	—	strong
RS121908531	DNM1L	—	—	strong
RS74315293	CPT2	—	—	strong
RS74315294	CPT2	—	—	strong
RS28936375	CPT2	—	—	strong
RS28936674	CPT2	—	—	strong
RS74315295	CPT2	—	—	strong
RS118204096	HMBS	—	—	strong
RS121918528	CPT2	—	—	strong
RS61750240	MECP2	—	—	strong
RS387907236	SERAC1	—	—	strong
RS772296795	SERAC1	—	—	strong
RS1199625391	SERAC1	—	—	strong
RS397509431	CPT2	—	—	strong
RS529232938	SERAC1	—	—	strong
RS515726173	CPT2	—	—	strong
RS515726177	CPT2	—	—	strong
RS186044004	CPT2	—	—	strong
RS267608615	MECP2	—	—	strong

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