Complex Neurodevelopmental Disorder

Other 285 variants 7 genes

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Associated Genes (7)

KCNQ2 SYNGAP1 EEF1A2 SCN2A SCN8A DYRK1A ANK2

Associated Variants (285)

RSID	Gene	Risk Allele	Odds Ratio	Evidence
RS794727134	KCNQ2	—	—	strong
RS397514741	SYNGAP1	—	—	strong
RS587777162	EEF1A2	—	—	strong
RS587780448	SCN2A	—	—	strong
RS184769423	SCN2A	—	—	strong
RS587780450	SCN2A	—	—	strong
RS587780455	SCN8A	—	—	strong
RS587780586	SCN8A	—	—	strong
RS587777721	SCN8A	—	—	strong
RS724159953	DYRK1A	—	—	strong
RS727503974	KCNQ2	—	—	strong
RS876657399	SCN8A	—	—	strong
RS863223345	SCN8A	—	—	strong
RS397514738	SCN8A	—	—	strong
RS794727152	SCN2A	—	—	strong
RS794727444	SCN2A	—	—	strong
RS794727813	KCNQ2	—	—	strong
RS797044521	DYRK1A	—	—	strong
RS796053171	SCN2A	—	—	strong
RS181327458	SCN2A	—	—	strong
RS796053175	SCN2A	—	—	strong
RS796053180	SCN2A	—	—	strong
RS796053182	SCN2A	—	—	strong
RS796053183	SCN2A	—	—	strong
RS2495911542	ANK2	—	—	strong
RS118192204	KCNQ2	—	—	strong
RS74315390	KCNQ2	—	—	strong
RS28939684	KCNQ2	—	—	strong
RS74315391	KCNQ2	—	—	strong
RS118192200	KCNQ2	—	—	strong
RS121917749	SCN2A	—	—	strong
RS121917750	SCN2A	—	—	strong
RS121917752	SCN2A	—	—	strong
RS121917753	SCN2A	—	—	strong
RS117067974	KCNQ2	—	—	strong
RS118192235	KCNQ2	—	—	strong
RS118192199	KCNQ2	—	—	strong
RS118192202	KCNQ2	—	—	strong
RS28939683	KCNQ2	—	—	strong
RS118192205	KCNQ2	—	—	strong
RS118192211	KCNQ2	—	—	strong
RS118192215	KCNQ2	—	—	strong
RS118192216	KCNQ2	—	—	strong
RS387906683	SCN2A	—	—	strong
RS387906684	SCN2A	—	—	strong
RS387906685	SCN2A	—	—	strong
RS387906686	SCN2A	—	—	strong
RS387906687	SCN2A	—	—	strong
RS202151337	SCN8A	—	—	strong
RS397514670	SYNGAP1	—	—	strong

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