DisGeNET - a database of gene-disease associations

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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
rs2069705	IFNG-AS1 ; IFNG	0.695	0.440	12	68161231	intron variant	G/A;C	snv			19
rs3750920	TOLLIP	0.807	0.120	11	1288726	synonymous variant	C/T	snv	0.40	0.38	7
rs5743899	TOLLIP ; LOC105376512	0.807	0.160	11	1302334	intron variant	C/T	snv		0.71	6