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
240724065050_4ihy	GeneSymbol	CFTR	NGG	install
240626183034_ii1p	AlleleID	929884	NGG	install
240619133208_edbx	GeneID	148398	NGG	install
240614073153_owax	GeneSymbol	SAMD11	NGG	install
240614004928_lcsi	AlleleID	30441	NGG	install
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