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
231124165432_8n05	GeneSymbol	SAMD11	NGG	install
231124165357_kaq0	GeneID	148398	NGG	install
231124133108_o54u	AlleleID	929884	NGG	install
231124133032_15w5	GeneSymbol	SAMD11	NGG	install
231121044730_ztaz	AlleleID	48221	NGG	install
231121040927_kyed	GeneSymbol	SLC6A1	NGG	install
231121040831_ukbd	GeneID	6529	NGG	install
231121035817_hi56	GeneID	148398	NGG	install
231113192748_1ywq	GeneSymbol	OPTN	NGG	correct
231113192724_1fm5	GeneSymbol	OPTN	NGG	install