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
231218165911_qdw8	AlleleID	15447	NGG	correct
231215130350_uhmp	GeneSymbol	SNCA	NGG	install
231215130335_oamm	GeneSymbol	SNCA	NGG	install
231215125813_kegp	GeneSymbol	SNCA	NGG	install
231213053157_li90	AlleleID	414728	NGG	install
231213053144_65qr	AlleleID	48221	NGG	install
231213053041_44al	AlleleID	48259	NGG	install
231213052639_pq1f	AlleleID	48221	NGG	install
231213052606_5ylj	AlleleID	48259	NGG	install
231213052500_rsy2	AlleleID	48221	NGG	install