DisGeNET - a database of gene-disease associations

Source: ALL

Results per page

Gene

Disease

Variant

Source

DSI _v

DPI _v

pLI

Consequence

AF_EXOME

AF_GENOME

Variant	Gene	Chr	Position	Consequence	Alleles	Class	AF GENOME	Num. diseases
rs1744297	ASPG	14	104102135	intron variant	T/C	snv	0.86	12
rs2238732	PRODH	22	18927834	intron variant	C/G;T	snv		7
rs17450273		12	102967601	intergenic variant	C/A;T	snv		4