DisGeNET - a database of gene-disease associations

List of associated variants

Coronary Artery Disease, C1956346

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
rs1412829	CDKN2B-AS1	0.742	0.400	9	22043927	intron variant	A/G	snv		0.28	6
rs2001844		0.882	0.040	8	125466503	upstream gene variant	A/G	snv		0.43	6
rs6859	NECTIN2	0.827	0.120	19	44878777	3 prime UTR variant	A/G	snv		0.58	6
rs20541	IL13 ; TH2LCRR	0.585	0.720	5	132660272	missense variant	A/G	snv	0.72	0.77	5
rs523096	CDKN2B-AS1	0.827	0.080	9	22019130	intron variant	A/G	snv		0.30	5
rs7049105	CDKN2B-AS1	0.807	0.120	9	22028802	intron variant	A/G	snv		0.58	5
rs867186	PROCR ; MMP24-AS1-EDEM2	0.752	0.120	20	35176751	missense variant	A/G	snv	0.10	9.7E-02	5
rs10757278	CDKN2B-AS1	0.620	0.520	9	22124478	intron variant	A/G	snv		0.40	4
rs10774625	ATXN2	0.763	0.320	12	111472415	intron variant	A/G	snv		0.66	4
rs10965219	CDKN2B-AS1	0.882	0.080	9	22053688	intron variant	A/G	snv		0.58	4
rs11066301	PTPN11	0.827	0.200	12	112433568	intron variant	A/G	snv		0.30	4
rs1333042	CDKN2B-AS1	0.827	0.120	9	22103814	intron variant	A/G	snv		0.63	4
rs2244608	HNF1A ; HNF1A-AS1	0.882	0.160	12	120979185	intron variant	A/G	snv		0.29	4
rs268	LPL	0.637	0.480	8	19956018	missense variant	A/G	snv	1.3E-02	1.3E-02	4
rs2681472	ATP2B1	0.882	0.080	12	89615182	intron variant	A/G	snv		0.14	4
rs611917	CELSR2	1.000	0.040	1	109272630	non coding transcript exon variant	A/G	snv	0.28	0.32	4
rs9349379	PHACTR1	0.732	0.200	6	12903725	intron variant	A/G	snv		0.32	4
rs1004467	CYP17A1 ; CYP17A1-AS1	0.790	0.280	10	102834750	non coding transcript exon variant	A/G	snv	0.15	0.14	3
rs16948048	ZNF652 ; LOC102724596	0.925	0.040	17	49363104	intron variant	A/G	snv		0.37	3
rs17114036	PLPP3	0.851	0.120	1	56497149	intron variant	A/G	snv		0.11	3
rs2303790	CETP	0.724	0.280	16	56983380	missense variant	A/G	snv	2.6E-03	6.5E-04	3
rs2383206	CDKN2B-AS1	0.742	0.320	9	22115027	intron variant	A/G	snv		0.49	3
rs2891168	CDKN2B-AS1	0.851	0.160	9	22098620	intron variant	A/G	snv		0.40	3
rs4773144	COL4A1 ; COL4A2	0.827	0.080	13	110308365	intron variant	A/G	snv		0.42	3
rs507666	ABO	1.000	0.040	9	133273983	intron variant	A/G	snv			3