DisGeNET - a database of gene-disease associations

List of associated variants

Coronary Artery Disease, C1956346

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
rs1051009	CXCL16	1.000	0.040	17	4734591	3 prime UTR variant	G/A	snv	0.35	0.27	1
rs10512861	DNAJC13	1.000	0.040	3	132539117	downstream gene variant	G/A;T	snv			1
rs1051338	LIPA	0.807	0.120	10	89247603	missense variant	T/G	snv	0.32	0.26	7
rs1051339	LIPA	0.882	0.040	10	89247582	missense variant	C/T	snv	9.5E-02	0.13	3
rs1051931	PLA2G7	0.708	0.400	6	46705206	missense variant	A/G	snv	0.81	0.79	19
rs1052133	OGG1 ; CAMK1	0.476	0.800	3	9757089	missense variant	C/G	snv	0.27	0.22	147
rs1056515	RGS5	0.882	0.040	1	163143470	3 prime UTR variant	G/T	snv		0.37	3
rs1056654	MPHOSPH6	0.925	0.160	16	82148406	3 prime UTR variant	G/A	snv		0.14	2
rs1056675	MPHOSPH6	0.925	0.160	16	82148329	3 prime UTR variant	T/A;C	snv			2
rs1057035	DICER1	0.763	0.440	14	95087805	3 prime UTR variant	T/C	snv		0.26	12
rs1057897	UBE2Z	1.000	0.040	17	48928147	3 prime UTR variant	T/A;G	snv			1
rs1058930	CYP2C8	0.882	0.040	10	95058362	missense variant	G/A;C	snv	1.0E-04; 3.7E-02		4
rs1061170	CFH	0.561	0.720	1	196690107	missense variant	C/T	snv	0.68	0.64	72
rs1063856	VWF	0.763	0.400	12	6044368	missense variant	T/C;G	snv	0.31		14
rs1065297	CXCL12	0.925	0.040	10	44370528	3 prime UTR variant	A/G	snv		5.4E-02	3
rs1065852	NDUFA6-DT ; LOC112268294 ; CYP2D6	0.695	0.360	22	42130692	missense variant	G/A	snv	0.21	0.19	19
rs10734649	SBF2-AS1 ; LINC02709	1.000	0.040	11	9759344	intron variant	C/A;G;T	snv			1
rs10738607	CDKN2B-AS1	0.925	0.080	9	22088095	intron variant	A/G	snv		0.42	4
rs10738610	CDKN2B-AS1	0.882	0.120	9	22123767	intron variant	A/C;T	snv			5
rs10740055	ARID5B	0.790	0.240	10	61958720	intron variant	C/A	snv		0.49	7
rs10741657	CYP2R1	0.637	0.520	11	14893332	upstream gene variant	A/G	snv		0.65	34
rs10754558	NLRP3	0.695	0.480	1	247448734	3 prime UTR variant	G/C;T	snv			20
rs10755578	LPA	0.925	0.040	6	160548706	intron variant	C/G	snv	0.44	0.42	2
rs10757264	CDKN2B-AS1	1.000	0.040	9	22019733	intron variant	A/G	snv		0.58	2
rs10757274	CDKN2B-AS1	0.701	0.320	9	22096056	intron variant	A/G	snv		0.41	22