DisGeNET - a database of gene-disease associations

List of associated variants

Coronary Arteriosclerosis, C0010054

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
rs12740374	CELSR2	0.851	0.040	1	109274968	3 prime UTR variant	G/T	snv		0.22	16
rs11014166	CACNB2	0.882	0.040	10	18419869	intron variant	A/T	snv		0.27	10
rs5880	CETP	0.827	0.040	16	56981179	missense variant	G/C	snv	5.2E-02	3.7E-02	10
rs2001844		0.882	0.040	8	125466503	upstream gene variant	A/G	snv		0.43	9
rs2144300	GALNT2	0.882	0.040	1	230159169	intron variant	C/T	snv		0.44	7
rs216311	VWF	0.882	0.040	12	6019277	missense variant	T/A;C	snv	4.0E-06; 0.69		7
rs342293	CTB-30L5.1	0.882	0.040	7	106731773	intron variant	C/G	snv		0.42	7
rs2306235	PLEKHO1	0.827	0.040	1	150150942	missense variant	C/G;T	snv	1.1E-02; 1.6E-05	4.4E-03	6
rs3900940	MYH15	0.827	0.040	3	108428881	missense variant	T/A;C	snv	4.3E-06; 0.24		6
rs11057830	SCARB1	0.851	0.040	12	124822507	intron variant	G/A	snv		0.15	5
rs1384889210	APOA1 ; APOA1-AS	0.827	0.040	11	116836193	missense variant	C/A	snv			5
rs2298566	SNX19	0.827	0.040	11	130880747	missense variant	A/C;T	snv	0.77; 4.0E-06		5
rs3828599	GPX3 ; LOC105378228	0.882	0.040	5	151022235	intron variant	A/G	snv		0.67	5
rs763802417	NOX1	0.882	0.040	X	100862805	missense variant	G/A	snv	5.9E-06		5
rs9332978	CYP4A11	0.882	0.040	1	46942278	upstream gene variant	T/C	snv		7.3E-02	5
rs1058930	CYP2C8	0.882	0.040	10	95058362	missense variant	G/A;C	snv	1.0E-04; 3.7E-02		4
rs116092985	PKD1	0.882	0.040	16	2110972	missense variant	A/G	snv	6.5E-02	7.8E-02	4
rs1199475313	ADRB3	0.851	0.040	8	37966277	missense variant	T/C	snv		7.0E-06	4
rs13144478		0.882	0.040	4	115275150	regulatory region variant	A/T	snv		5.5E-02	4
rs142677199	ACE	0.882	0.040	17	63479897	missense variant	G/A;T	snv	3.2E-05		4
rs1790349	DHCR7	0.882	0.040	11	71431304	intron variant	T/C	snv		0.19	4
rs180070	LINC01497	0.882	0.040	17	69960745	upstream gene variant	G/T	snv		0.77	4
rs2015086	CCL18	0.882	0.040	17	36064257	upstream gene variant	A/G	snv		0.22	4
rs3931020		0.882	0.040	1	74769633	downstream gene variant	T/C	snv		0.71	4
rs4888378	CFDP1	0.851	0.040	16	75298143	intron variant	A/G	snv		0.52	4