DisGeNET - a database of gene-disease associations

List of associated variants

Coronary Artery Disease, C1956346

Source: GWASCAT ×

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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
rs1378942	CSK	0.790	0.240	15	74785026	intron variant	C/A;T	snv			6
rs12423664	FBRSL1	1.000	0.040	12	132493308	intron variant	G/A	snv		0.10	6
rs2521501	FES	0.925	0.080	15	90894158	intron variant	A/C;T	snv			6
rs2244608	HNF1A ; HNF1A-AS1	0.882	0.160	12	120979185	intron variant	A/G	snv		0.29	6
rs7209400	LOC102724596	1.000	0.040	17	49372695	intron variant	C/T	snv		0.47	6
rs4299376	LOC102725159 ; ABCG8	0.851	0.120	2	43845437	intron variant	G/C;T	snv			6
rs11172113	LRP1	0.882	0.080	12	57133500	intron variant	T/C	snv		0.42	6
rs17608766	LRRC37A2 ; GOSR2	1.000	0.040	17	46935905	3 prime UTR variant	T/C	snv		9.2E-02	6
rs11591147	PCSK9	0.677	0.360	1	55039974	missense variant	G/A;T	snv	1.2E-02		6
rs867186	PROCR ; MMP24-AS1-EDEM2	0.752	0.120	20	35176751	missense variant	A/G	snv	0.10	9.7E-02	6
rs599839	PSRC1	0.724	0.360	1	109279544	downstream gene variant	G/A;C	snv			6
rs56062135	SMAD3	0.790	0.200	15	67163292	intron variant	C/T	snv		0.18	6
rs72743461	SMAD3	0.827	0.160	15	67149412	intron variant	C/A;T	snv			6
rs4986790	TLR4	0.438	0.800	9	117713024	missense variant	A/G;T	snv	6.1E-02; 4.0E-06		6
rs2943634		0.763	0.200	2	226203364	intergenic variant	A/C;G	snv			5
rs2943641		0.763	0.160	2	226229029	intergenic variant	T/C	snv		0.67	5
rs2231142	ABCG2	0.583	0.680	4	88131171	missense variant	G/C;T	snv	4.0E-06; 0.12		5
rs445925	APOC1	0.882	0.080	19	44912383	non coding transcript exon variant	G/A;C	snv			5
rs6265	BDNF ; BDNF-AS	0.436	0.760	11	27658369	missense variant	C/T	snv	0.19	0.15	5
rs4977756	CDKN2B-AS1	0.683	0.440	9	22068653	intron variant	G/A	snv		0.64	5
rs1061170	CFH	0.561	0.720	1	196690107	missense variant	C/T	snv	0.68	0.64	5
rs1004467	CYP17A1 ; CYP17A1-AS1	0.790	0.280	10	102834750	non coding transcript exon variant	A/G	snv	0.15	0.14	5
rs1250259	FN1 ; LOC105373868	1.000	0.040	2	215435759	missense variant	T/A	snv	0.76	0.79	5
rs17514846	FURIN	0.882	0.120	15	90873320	intron variant	C/A;G	snv			5
rs10774624	LINC02356	0.882	0.160	12	111395984	intron variant	G/A	snv		0.67	5