Chromatinopathy

Other 8 variants 8 genes

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Associated Genes (8)

TFAP2A SETD5 CHD7 KAT6B MED13L ANKRD11 EFTUD2 KANSL1

Associated Variants (8)

RSID	Gene	Risk Allele	Odds Ratio	Evidence
RS121909574	TFAP2A	—	—	strong
RS2041379870	SETD5	—	—	strong
RS1804098617	CHD7	—	—	strong
RS1846182844	KAT6B	—	—	strong
RS1877531485	MED13L	—	—	strong
RS2035028859	ANKRD11	—	—	strong
RS2050609487	EFTUD2	—	—	strong
RS2078389049	KANSL1	—	—	strong