DisGeNET - a database of gene-disease associations

List of shared variants

Coronary Arteriosclerosis, C0010054

Disease: Hypertensive disease

Source: ALL

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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
rs142677199	ACE	0.882	0.040	17	63479897	missense variant	G/A;T	snv	3.2E-05		4
rs180070	LINC01497	0.882	0.040	17	69960745	upstream gene variant	G/T	snv		0.77	4
rs553350297	AGTR1	0.882	0.040	3	148741588	missense variant	G/A	snv	1.2E-05	2.1E-05	4
rs761401927	ACE	0.882	0.040	17	63488704	missense variant	G/A	snv	9.1E-05		4
rs762079672	AGT	0.882	0.040	1	230710211	missense variant	C/T	snv	4.0E-06		4
rs897876		0.882	0.040	2	65564447	intron variant	C/T	snv		0.30	4
rs3828599	GPX3 ; LOC105378228	0.882	0.040	5	151022235	intron variant	A/G	snv		0.67	5
rs9332978	CYP4A11	0.882	0.040	1	46942278	upstream gene variant	T/C	snv		7.3E-02	5
rs2306235	PLEKHO1	0.827	0.040	1	150150942	missense variant	C/G;T	snv	1.1E-02; 1.6E-05	4.4E-03	6
rs529038	ROS1	0.827	0.120	6	117301070	missense variant	C/G;T	snv	0.20	0.19	6
rs7195830	CYBA	0.851	0.080	16	88643304	3 prime UTR variant	A/G	snv	0.62	0.69	6
rs10118757	MTAP	0.827	0.120	9	21853340	intron variant	A/G	snv		0.26	7
rs2144300	GALNT2	0.882	0.040	1	230159169	intron variant	C/T	snv		0.44	7
rs771676129	CD36	0.827	0.080	7	80671082	synonymous variant	C/T	snv	4.0E-06		7
rs999947969	CD36	0.827	0.080	7	80671145	synonymous variant	C/T	snv			7
rs10509681	CYP2C8	0.807	0.160	10	95038992	missense variant	T/C	snv	8.3E-02	8.0E-02	8
rs2576178	RNLS ; LIPJ	0.790	0.160	10	88583641	5 prime UTR variant	A/G	snv		0.29	9
rs8259	BSG	0.776	0.200	19	582927	3 prime UTR variant	T/A	snv		0.39	9
rs11014166	CACNB2	0.882	0.040	10	18419869	intron variant	A/T	snv		0.27	10
rs41507953	EPHX2	0.790	0.280	8	27500988	missense variant	A/G	snv	8.7E-02	0.13	10
rs6903956	ADTRP	0.763	0.160	6	11774350	intron variant	A/G	snv		0.65	10
rs17465637	MIA3	0.790	0.200	1	222650187	intron variant	A/C;G;T	snv	0.64; 6.4E-06		11
rs185847354	ADIPOQ ; ADIPOQ-AS1	0.763	0.160	3	186854460	missense variant	T/C	snv	3.1E-04	7.0E-05	11
rs2106261	ZFHX3	0.763	0.160	16	73017721	intron variant	C/G;T	snv			11
rs1761667	CD36	0.752	0.320	7	80615623	intron variant	G/A	snv		0.49	12