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
231129101443_7b5s	AlleleID	32053	NGG	correct
231129101353_sggo	GeneSymbol	GJB2	NGG	correct
231129101331_ly8n	GeneSymbol	GJB2	NGG	correct
231127181048_z8l8	GeneSymbol	GPX4	NGG	install
231127175704_33mh	GeneSymbol	GPX4	NGG	install
231127175033_t4wh	GeneSymbol	GPX4	NGG	install
231127173020_4ila	GeneSymbol	GPX4	NGG	install
231124165652_euyc	GeneSymbol	SCD5	NGG	correct
231124165622_qp5u	GeneSymbol	SCD5	NGG	install
231124165537_wbma	GeneSymbol	SCD5	NGG	install