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
231105145953_fe8e	GeneID	5172	NGG	install
231105135215_c3kz	GeneID	351	NGG	correct
231105132133_nhjy	GeneID	2706	NGG	correct
231105131727_ttdd	AlleleID	929884	NGG	install
231104173925_xyrj	GeneID	3039	NGG	install
231104173834_z0zc	GeneID	3039	NGG	install
231104173834_gzl8	GeneID	3039	NGG	install
231104145644_4la1	AlleleID	929884	NGG	install
231103155457_599m	GeneID	148398	NGG	install
231102191534_f4q8	GeneSymbol	NF1	NGG	install