Developmental Delay

Other 222 variants 19 genes

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Associated Genes (19)

SOX4 KCNMA1 NFE2L2 ATN1 SRCAP MORC2 CSNK2B TUBGCP2 ARFGEF1 ASXL1 SLC25A22 GNAO1 CTBP1 TSHR SCN3A GRIN2B UBE3A CDKL5 NUP214

Associated Variants (222)

RSID	Gene	Risk Allele	Odds Ratio	Evidence
RS1582601669	SOX4	—	—	strong
RS762705295	KCNMA1	—	—	strong
RS1553487947	NFE2L2	—	—	strong
RS1553487942	NFE2L2	—	—	strong
RS1553488015	NFE2L2	—	—	strong
RS1484259264	KCNMA1	—	—	strong
RS1555144357	ATN1	—	—	strong
RS1555144358	ATN1	—	—	strong
RS1334099693	SOX4	—	—	strong
RS1565569158	ATN1	—	—	strong
RS777744269	SRCAP	—	—	strong
RS556230791	SRCAP	—	—	strong
RS1464282327	SOX4	—	—	strong
RS779992354	SRCAP	—	—	strong
RS1582601747	SOX4	—	—	strong
RS749265202	KCNMA1	—	—	strong
RS1602496057	MORC2	—	—	strong
RS1583610622	CSNK2B	—	—	strong
RS1328294721	KCNMA1	—	—	strong
RS1449999247	TUBGCP2	—	—	strong
RS200129338	TUBGCP2	—	—	strong
RS1589822227	TUBGCP2	—	—	strong
RS773890896	SRCAP	—	—	strong
RS139542422	SRCAP	—	—	strong
RS2491362882	ARFGEF1	—	—	strong
RS373677230	KCNMA1	—	—	strong
RS199469464	SRCAP	—	—	strong
RS373145711	ASXL1	—	—	strong
RS60216939	ATN1	—	—	strong
RS797044566	ATN1	—	—	strong
RS754606765	KCNMA1	—	—	strong
RS200175704	SRCAP	—	—	strong
RS183497403	SRCAP	—	—	strong
RS200603610	SLC25A22	—	—	strong
RS797044951	GNAO1	—	—	strong
RS864309503	MORC2	—	—	strong
RS864309504	MORC2	—	—	strong
RS869320802	CTBP1	—	—	strong
RS121908869	TSHR	—	—	strong
RS771334638	SRCAP	—	—	strong
RS186883352	SRCAP	—	—	strong
RS200403976	SRCAP	—	—	strong
RS139814474	SRCAP	—	—	strong
RS1057518801	SCN3A	—	—	strong
RS1057518800	GRIN2B	—	—	strong
RS1057518777	UBE3A	—	—	strong
RS1057518759	CDKL5	—	—	strong
RS1057519922	NFE2L2	—	—	strong
RS1064795559	MORC2	—	—	strong
RS1135402758	NUP214	—	—	strong

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