DisGeNET - a database of gene-disease associations

List of shared variants

Atherosclerosis, C0004153

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
rs212528	ECE1	0.925	0.040	1	21259168	intron variant	T/C	snv		0.12	3
rs213045	ECE1	0.851	0.120	1	21290752	intron variant	G/T	snv		0.44	5
rs2066715	ABCA1	0.807	0.160	9	104825752	missense variant	C/T	snv	8.2E-02	5.5E-02	7
rs3861950	TNFSF4	0.827	0.160	1	173187153	intron variant	T/C	snv		0.47	7
rs5351	EDNRB-AS1 ; EDNRB	0.807	0.240	13	77901178	synonymous variant	T/C;G	snv	0.57		7
rs1020608562	CCR5AS ; CCR5	0.807	0.160	3	46373738	missense variant	T/C	snv	4.0E-06		9
rs2972146		0.882	0.040	2	226235982	intergenic variant	G/T	snv		0.72	9
rs198389	NPPB	0.776	0.240	1	11859214	upstream gene variant	A/G	snv		0.39	10
rs6903956	ADTRP	0.763	0.160	6	11774350	intron variant	A/G	snv		0.65	10
rs1126478	LTF	0.763	0.240	3	46459723	missense variant	T/C	snv	0.41	0.51	11
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
rs549591993	F7	0.776	0.400	13	113105794	5 prime UTR variant	C/A	snv	4.0E-04	2.8E-05	12
rs2536512	SOD3	0.752	0.280	4	24799693	missense variant	G/A;T	snv	0.55		14
rs5355	C1orf112 ; SELE	0.742	0.240	1	169726729	missense variant	G/A	snv	4.5E-02	3.3E-02	14
rs1122608	SMARCA4	0.763	0.120	19	11052925	intron variant	G/T	snv		0.18	16
rs1378942	CSK	0.790	0.240	15	74785026	intron variant	C/A;T	snv			16
rs4606	RGS2	0.752	0.120	1	192812042	3 prime UTR variant	C/G;T	snv			16
rs5182	AGTR1	0.742	0.160	3	148741608	synonymous variant	C/T	snv	0.49	0.41	16
rs2071746	HMOX1	0.708	0.320	22	35380679	intron variant	A/T	snv		0.49	18
rs2943641		0.763	0.160	2	226229029	intergenic variant	T/C	snv		0.67	18
rs11556924	ZC3HC1	0.752	0.240	7	130023656	missense variant	C/A;T	snv	4.0E-06; 0.28		21
rs10757274	CDKN2B-AS1	0.701	0.320	9	22096056	intron variant	A/G	snv		0.41	22
rs3782886	BRAP	0.724	0.480	12	111672685	synonymous variant	T/C	snv	1.9E-02	5.9E-03	22