Welcome to OPEDVar!

Use an example AlleleID GeneID GeneSymbol HGNC_ID QUERY TYPE Select query type and 'AlleleID', 'GeneID', 'GeneSymbol' and 'HGNC_ID' QUERY ITEM Enter the AlleleID,GeneID,GeneSymbol or HGNC_ID PAM Select PAM type between 'NGG' and 'NG' DIRECTION Select edit direction which means to install or correct pathogenic human genetic variants ASSEMBLY

HISTORY

UID	Query Type	Query Item	PAM	Direction
240221050631_8ocn	GeneSymbol	CHD2	NGG	install
240122110300_9yqg	GeneSymbol	TINF2	NGG	install
240116033230_vakh	AlleleID	929884	NGG	install
240110013105_ec1p	HGNC_ID	17761	NGG	install
240105134125_mqev	GeneSymbol	PJVK	NGG	correct
240104210402_lz64	GeneSymbol	MTHFR	NGG	correct
240104145304_onrn	GeneSymbol	PJVK	NG	correct
240104145243_1hso	GeneSymbol	PJVK	NGG	install
240104144713_0v9e	GeneSymbol	PJVK	NGG	correct
240103132153_ex3l	AlleleID	929884	NGG	install