DisGeNET - a database of gene-disease associations

List of shared variants

Blood Pressure, C0005823

Disease: Hypertensive disease

Source: GWASDB ×

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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
rs1799945	LOC108783645 ; HFE	0.452	0.760	6	26090951	missense variant	C/G;T	snv	0.11	0.10	10
rs13107325	SLC39A8	0.776	0.520	4	102267552	missense variant	C/A;T	snv	4.0E-06; 4.5E-02		8
rs11014166	CACNB2	0.882	0.040	10	18419869	intron variant	A/T	snv		0.27	5
rs2521501	FES	0.925	0.080	15	90894158	intron variant	A/C;T	snv			5
rs1173771				5	32814922	regulatory region variant	A/G	snv		0.65	4
rs2681472	ATP2B1	0.882	0.080	12	89615182	intron variant	A/G	snv		0.14	4
rs6015450	ZNF831			20	59176062	intron variant	A/G	snv		0.14	4
rs633185	ARHGAP42	0.925	0.080	11	100722807	intron variant	G/A;C	snv			4
rs932764	PLCE1			10	94136183	intron variant	A/G	snv		0.38	4