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
rs763802417	NOX1	0.882	0.040	X	100862805	missense variant	G/A	snv	5.9E-06		5
rs1065852	NDUFA6-DT ; LOC112268294 ; CYP2D6	0.695	0.360	22	42130692	missense variant	G/A	snv	0.21	0.19	19
rs4818	COMT ; MIR4761	0.683	0.440	22	19963684	synonymous variant	C/G;T	snv	0.34		27
rs755622	MIF-AS1 ; MIF	0.611	0.720	22	23894205	intron variant	G/C	snv		0.26	44
rs2254638	N6AMT1	0.882	0.040	21	28883961	intron variant	A/C;G	snv			3
rs428785	ADAMTS1	0.882	0.040	21	26844276	missense variant	C/A;G;T	snv	1.3E-05; 0.70	0.78	3
rs1042579	THBD	0.732	0.240	20	23048087	missense variant	G/A;T	snv	0.19		16
rs1223493898	HNF4A	0.851	0.120	20	44406090	missense variant	G/A;C	snv			5
rs147377392	THBD	0.763	0.120	20	23048144	missense variant	A/G	snv	1.0E-04	2.8E-04	11
rs16998248	ZNF217	0.882	0.040	20	53581801	synonymous variant	T/A	snv	0.11	8.8E-02	3
rs17576	MMP9	0.557	0.760	20	46011586	missense variant	A/G	snv	0.39	0.36	73
rs35720349	ZNF217	0.882	0.040	20	53577121	missense variant	G/A	snv	3.4E-02	1.6E-02	3
rs3746444	MIR499A ; MIR499B ; MYH7B ; LOC107985393	0.514	0.760	20	34990448	mature miRNA variant	A/G	snv	0.20	0.19	105
rs3918242	MMP9	0.602	0.680	20	46007337	upstream gene variant	C/T	snv		0.14	54
rs753630955	TGM2	0.882	0.040	20	38161510	stop gained	G/A;T	snv	2.0E-05		3
rs901895948	TGM2	0.882	0.040	20	38131160	missense variant	C/T	snv			3
rs911119	CST3	0.807	0.120	20	23632100	non coding transcript exon variant	C/G;T	snv			9
rs1035071612	MIR6886 ; LDLR	0.763	0.240	19	11113361	missense variant	C/A;T	snv	4.0E-06		9
rs1122608	SMARCA4	0.763	0.120	19	11052925	intron variant	G/T	snv		0.18	16
rs11542041	APOE	0.677	0.480	19	44908690	missense variant	C/A;T	snv		2.1E-05	23
rs11615	ERCC1	0.572	0.640	19	45420395	synonymous variant	A/G	snv	0.50	0.55	62
rs116843064	ANGPTL4	0.776	0.160	19	8364439	missense variant	G/A	snv	1.3E-02	1.5E-02	16
rs1181860747	INSR	0.776	0.240	19	7122961	missense variant	C/T	snv			10
rs12979860	IFNL4	0.547	0.520	19	39248147	intron variant	C/T	snv		0.39	84
rs1310478538	C3	0.851	0.080	19	6713295	missense variant	C/G	snv		1.4E-05	4