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
260402170654_bs6k	GeneSymbol	LMNA	NG	correct
260402170528_u5l3	GeneSymbol	LMNA	NG	correct
260402170519_e8k4	GeneID	4000	NG	correct
260328024544_meht	GeneSymbol	DEAF1	NG	correct
260328024507_p0xb	GeneSymbol	DEAF1	NG	correct
260328024221_cmrk	GeneSymbol	DEAF1	NGG	correct
260323111209_fznz	GeneSymbol	TMEM70	NGG	install
260323111129_5j5h	GeneSymbol	SAMD11	NGG	install
260227173640_ajy8	GeneSymbol	SAMD11	NGG	install
251229212515_52yl	AlleleID	29732	NGG	correct