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
230711232017_1wyt	AlleleID	526296	NGG	install
230705085630_avbz	GeneSymbol	SAMD11	NGG	install
230704111347_85k0	HGNC_ID	28706	NGG	install
230704111342_xokw	GeneSymbol	SAMD11	NGG	install
230704111333_8bac	GeneID	148398	NGG	install
230704082607_o9je	GeneID	148398	NGG	install
230704081710_80u5	HGNC_ID	28706	NGG	install
230704081617_bef8	GeneSymbol	SAMD11	NGG	install
230630164816_ofhh	GeneSymbol	SAMD11	NGG	install
230630153942_wbmp	GeneSymbol	SAMD11	NGG	install