DisGeNET - a database of gene-disease associations

List of associated variants

Alanine measurement, C0523459

Source: ALL

Results per page

Gene

Disease

Variant

Source

DSI _v

DPI _v

pLI

Consequence

AF_EXOME

AF_GENOME

Variant	Gene	DSI _v	DPI _v	Chr	Position	Consequence	Alleles	Class	AF EXOME	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
rs588682	DLGAP1			18	3558080	intron variant	G/A	snv		0.71	2