Neurodevelopmental Abnormality

Other 103 variants 35 genes

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Associated Genes (35)

PRMT9 TCF7L2 CDK13 ZMYM2 CAMTA1 ANKRD11 ARID1B GRIN2A SPTAN1 NCKAP1 CREBBP AGO1 MYT1L CUL3 NGLY1 SETD5 SEPSECS KMT2C AUTS2 STX1A GNAI1 PUF60 ZMIZ1 AHDC1 PRMT7 KDM6B SMG9 ASXL1 TCF20 MSL3 GRIA3 DDX3X TFE3 NIPBL CACNA1A

Associated Variants (103)

RSID	Gene	Risk Allele	Odds Ratio	Evidence
RS2530575861	PRMT9	—	—	strong
RS2137178800	TCF7L2	—	—	strong
RS2150517037	CDK13	—	—	strong
RS765831882	ZMYM2	—	—	strong
RS2149303071	CAMTA1	—	—	strong
RS759375404	PRMT9	—	—	strong
RS769164317	PRMT9	—	—	strong
RS2530677875	PRMT9	—	—	strong
RS780261399	PRMT9	—	—	strong
RS142189908	PRMT9	—	—	strong
RS2530696820	PRMT9	—	—	strong
RS1394475208	PRMT9	—	—	strong
RS1733174455	PRMT9	—	—	strong
RS2151736830	ANKRD11	—	—	strong
RS1392285676	PRMT9	—	—	strong
RS2530696627	PRMT9	—	—	strong
RS756105948	PRMT9	—	—	strong
RS747281440	PRMT9	—	—	strong
RS748127912	PRMT9	—	—	strong
RS2530679409	PRMT9	—	—	strong
RS141216537	PRMT9	—	—	strong
RS2546839479	ARID1B	—	—	strong
RS2506111451	GRIN2A	—	—	strong
RS2541012589	SPTAN1	—	—	strong
RS2468604532	NCKAP1	—	—	strong
RS2051853150	CREBBP	—	—	strong
RS1645264815	AGO1	—	—	strong
RS2048967703	MYT1L	—	—	strong
RS1692821396	CUL3	—	—	strong
RS762276611	NGLY1	—	—	strong
RS2045187265	SETD5	—	—	strong
RS748528138	SEPSECS	—	—	strong
RS2093231242	KMT2C	—	—	strong
RS1789934246	AUTS2	—	—	strong
RS200456346	STX1A	—	—	strong
RS1787388036	GNAI1	—	—	strong
RS1816304706	PUF60	—	—	strong
RS1039220588	ZMIZ1	—	—	strong
RS2019544779	AHDC1	—	—	strong
RS2082897416	PRMT7	—	—	strong
RS957520585	KDM6B	—	—	strong
RS1968559161	SMG9	—	—	strong
RS2011867276	ASXL1	—	—	strong
RS1920931611	TCF20	—	—	strong
RS2053176048	MSL3	—	—	strong
RS2045826576	GRIA3	—	—	strong
RS2063928899	DDX3X	—	—	strong
RS2064742925	TFE3	—	—	strong
RS2149510283	NIPBL	—	—	strong
RS2145002387	CACNA1A	—	—	strong

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