DisGeNET - a database of gene-disease associations

List of shared variants

Coronary Artery Disease, C1956346

Disease: Hypertensive disease

Source: GWASCAT ×

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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
rs10857147		1.000	0.040	4	80259918	intergenic variant	A/T	snv		0.25	9
rs604723	ARHGAP42	1.000	0.040	11	100739815	intron variant	T/C	snv		0.78	8
rs633185	ARHGAP42	0.925	0.080	11	100722807	intron variant	G/A;C	snv			8
rs2681492	ATP2B1	0.925	0.040	12	89619312	intron variant	T/C;G	snv			7
rs2681472	ATP2B1	0.882	0.080	12	89615182	intron variant	A/G	snv		0.14	6
rs2972146		0.882	0.040	2	226235982	intergenic variant	G/T	snv		0.72	6
rs17514846	FURIN	0.882	0.120	15	90873320	intron variant	C/A;G	snv			5