History of Neurodevelopmental Disorder

Other 41 variants 30 genes

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Associated Genes (30)

KIF1A FANCB GRIA3 SYP ZNF41 OFD1 CHD2 SCN2A L1CAM KAT6A SRPX2 PAK3 FLNA MID1 DKC1 NDP SLC16A2 SYN1 ATRX ABCD1 ZNF674 FGD1 NRXN1 SMC1A TSPAN7 ATP7A ARHGEF6 ARX BCOR MED12

Associated Variants (41)

RSID	Gene	Risk Allele	Odds Ratio	Evidence
RS369849214	KIF1A	—	—	strong
RS145110602	FANCB	—	—	strong
RS151086692	GRIA3	—	—	strong
RS139475570	SYP	—	—	strong
RS144904486	ZNF41	—	—	strong
RS146251034	OFD1	—	—	strong
RS752940775	CHD2	—	—	strong
RS376658420	KIF1A	—	—	strong
RS1553567409	SCN2A	—	—	strong
RS527346259	KIF1A	—	—	strong
RS781908326	L1CAM	—	—	strong
RS142959373	FANCB	—	—	strong
RS762302738	KAT6A	—	—	strong
RS146063801	SRPX2	—	—	strong
RS1569398792	PAK3	—	—	strong
RS1382076574	FLNA	—	—	strong
RS374851071	MID1	—	—	strong
RS150319104	DKC1	—	—	strong
RS73475744	NDP	—	—	strong
RS201039304	SLC16A2	—	—	strong
RS772106134	SYN1	—	—	strong
RS143037290	KIF1A	—	—	strong
RS122445110	ATRX	—	—	strong
RS193922098	ABCD1	—	—	strong
RS200533370	SYN1	—	—	strong
RS201621696	ZNF674	—	—	strong
RS398124157	FGD1	—	—	strong
RS55923848	NRXN1	—	—	strong
RS143495349	NRXN1	—	—	strong
RS112536447	NRXN1	—	—	strong
RS112727682	SMC1A	—	—	strong
RS104894951	TSPAN7	—	—	strong
RS146692150	ATP7A	—	—	strong
RS141441058	KIF1A	—	—	strong
RS151195816	NRXN1	—	—	strong
RS147131853	ARHGEF6	—	—	strong
RS797045301	ARX	—	—	strong
RS139802143	BCOR	—	—	strong
RS757160341	MED12	—	—	strong
RS199574770	KIF1A	—	—	strong
RS375972461	KIF1A	—	—	strong