DisGeNET - a database of gene-disease associations

List of shared variants

Coronary Arteriosclerosis, C0010054

Disease: Coronary Artery 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
rs189970623	CYP2B6	0.882	0.040	19	41009368	missense variant	C/A;G;T	snv	3.0E-04		3
rs2043211	CARD8	0.653	0.480	19	48234449	missense variant	A/T	snv	0.33	0.29	29
rs2228671	LDLR	0.790	0.160	19	11100236	stop gained	C/A;G;T	snv	1.6E-05; 8.9E-02		14
rs2288904	SLC44A2	0.807	0.240	19	10631494	missense variant	A/G	snv	0.80	0.83	8
rs25487	XRCC1	0.441	0.800	19	43551574	missense variant	T/C	snv	0.68	0.71	205
rs267606661	APOE	0.763	0.120	19	44909101	missense variant	C/G;T	snv	3.9E-04; 1.0E-05		10
rs352493	SIRT6 ; ANKRD24	0.882	0.040	19	4180839	missense variant	C/G;T	snv	0.88		3
rs3760908	ANKRD24 ; SIRT6	0.882	0.040	19	4184515	intron variant	A/G	snv		0.18	3
rs4420638	APOC1	0.708	0.520	19	44919689	downstream gene variant	A/G	snv		0.18	43
rs544456198	LDLR	0.790	0.120	19	11116930	missense variant	G/T	snv	8.0E-06	2.8E-05	9
rs5498	ICAM4 ; ICAM1	0.531	0.760	19	10285007	missense variant	A/G	snv	0.44	0.37	99
rs6511720	LDLR	0.790	0.120	19	11091630	intron variant	G/T	snv		0.12	15
rs6859	NECTIN2	0.827	0.120	19	44878777	3 prime UTR variant	A/G	snv		0.58	10
rs688	LDLR	0.742	0.400	19	11116926	synonymous variant	C/T	snv	0.39	0.34	16
rs72658855	LDLR	0.882	0.040	19	11100245	missense variant	C/G;T	snv	2.3E-03	9.4E-03	3
rs752596535	LDLR	0.752	0.200	19	11105407	stop gained	C/A;G;T	snv	1.6E-05		14
rs764929617	APOE	0.776	0.200	19	44907799	missense variant	C/T	snv	4.0E-06		8
rs8259	BSG	0.776	0.200	19	582927	3 prime UTR variant	T/A	snv		0.39	9
rs9797861	SLC44A2	0.790	0.200	19	10632450	intron variant	C/A;G;T	snv			9
rs17757541	BCL2	0.827	0.240	18	63212453	intron variant	C/G;T	snv			7
rs2000813	LIPG	0.763	0.200	18	49567494	missense variant	C/A;T	snv	4.0E-06; 0.27; 4.0E-06	0.23	9
rs770572030	LIPG	0.827	0.160	18	49581427	missense variant	T/A;C	snv	4.0E-06; 4.0E-06		5
rs1042522	TP53	0.426	0.800	17	7676154	missense variant	G/C;T	snv	0.67		242
rs112735431	RNF213 ; RNF213-AS1	0.683	0.320	17	80385145	missense variant	G/A;C	snv	2.6E-04; 8.0E-06		24
rs1129844	CCL11	0.752	0.320	17	34285875	missense variant	G/A;C;T	snv	0.16; 1.2E-05		13