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
230630153938_zebq	GeneSymbol	SAMD11	NGG	install
230630153938_s5n2	GeneSymbol	SAMD11	NGG	install
230630153938_h6je	GeneSymbol	SAMD11	NGG	install
230630153938_80ih	GeneSymbol	SAMD11	NGG	install
230630153937_db7g	GeneSymbol	SAMD11	NGG	install
230630153934_3wk6	GeneSymbol	SAMD11	NGG	install
230630152454_8755	AlleleID	929884	NGG	install
230630152452_yjsb	HGNC_ID	28706	NGG	install
230630152449_vs89	GeneSymbol	SAMD11	NGG	install
230630152443_je3n	GeneSymbol	SAMD11	NGG	install