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
241017172915_73tr	GeneSymbol	GJB2	NGG	correct
240912030715_2yvk	GeneID	148398	NGG	install
240829121522_ia7j	GeneSymbol	ERCC4	NGG	install
240829121426_gv6b	GeneSymbol	ERCC4	NGG	install
240826233018_k0mt	GeneSymbol	GBA	NGG	install
240819053248_kgtw	GeneSymbol	NRAS	NGG	install
240819052556_kvs1	AlleleID	929884	NGG	install
240819052535_r2v5	GeneSymbol	NRAS	NGG	install
240724065050_4ihy	GeneSymbol	CFTR	NGG	install
240626183034_ii1p	AlleleID	929884	NGG	install