Disease table of EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 2 OMIM ID: 607681

Gene-disease associations table

Gene	Associated with EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 2 in	Link to HGNC	Cytogenetic band	Number of associated diseases	Associated diseases
GABRG2	ClinVar, OMIM, HUMSAVAR	HGNC link	5q34	3	PS121210, 607681, PS604233