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
250806105403_dk0s	GeneID	7157	NGG	install
250730224234_cebw	GeneSymbol	ATR	NGG	install
250711095234_7jmn	GeneSymbol	LMNA	NGG	install
250519013652_8tuv	GeneID	148398	NGG	install
250519013005_ct5w	GeneID	148398	NGG	install
250428134436_bzi9	GeneID	148398	NGG	install
250428134435_kzac	GeneID	148398	NGG	install
250409082940_6pas	GeneSymbol	JAK2	NGG	install
250409075152_qxs2	AlleleID	929884	NGG	correct
250403213809_ahfu	HGNC_ID	6893	NGG	install