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
240614004822_7jhs	GeneSymbol	HBB	NGG	install
240614004447_ervz	GeneSymbol	HBB	NGG	install
240613064821_03um	GeneSymbol	PUM1	NGG	install
240613064637_afhi	HGNC_ID	14957	NGG	install
240613064529_yatm	AlleleID	929884	NGG	install
240605131821_awov	GeneSymbol	CFTR	NGG	correct
240601235656_ajkt	GeneSymbol	SAMD11	NGG	install
240530234603_3nq9	AlleleID	264183	NGG	correct
240530234547_f5sl	AlleleID	264183	NGG	install
240530234531_x0vo	AlleleID	264183	NGG	correct