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
231102022245_iphz	GeneSymbol	HEXA	NGG	install
231102022234_rn43	GeneSymbol	HEXA	NGG	install
231102015809_d96m	GeneSymbol	HEXA	NGG	install
231102015324_mnrg	GeneSymbol	HEXA	NGG	install
231030125057_5ac7	GeneSymbol	SAMD11	NGG	install
231029154056_vbys	GeneSymbol	PLN	NGG	correct
231029154003_b0h5	GeneSymbol	PLN	NGG	install
231029153737_z4cc	GeneSymbol	PLN	NGG	install
230819164256_zxjo	AlleleID	929884	NGG	install
230819164241_kgy3	HGNC_ID	329	NGG	correct