DisGeNET - a database of gene-disease associations

List of shared variants

Coronary Artery Disease, C1956346

Disease: Cardiovascular Diseases

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
rs3184504	SH2B3 ; ATXN2	0.572	0.600	12	111446804	missense variant	T/A;C;G	snv	0.67		61
rs964184	ZPR1	0.716	0.440	11	116778201	3 prime UTR variant	G/C	snv		0.82	35
rs7412	APOE	0.641	0.640	19	44908822	missense variant	C/T	snv	6.2E-02	7.9E-02	20
rs11556924	ZC3HC1	0.752	0.240	7	130023656	missense variant	C/A;T	snv	4.0E-06; 0.28		13
rs28601761		1.000	0.040	8	125487789	intron variant	C/G	snv		0.37	13
rs12740374	CELSR2	0.851	0.040	1	109274968	3 prime UTR variant	G/T	snv		0.22	9
rs3918226	NOS3	0.925	0.080	7	150993088	intron variant	C/T	snv		5.7E-02	9
rs604723	ARHGAP42	1.000	0.040	11	100739815	intron variant	T/C	snv		0.78	8
rs6905288		0.882	0.120	6	43791136	downstream gene variant	G/A	snv		0.56	8
rs2681492	ATP2B1	0.925	0.040	12	89619312	intron variant	T/C;G	snv			7
rs11591147	PCSK9	0.677	0.360	1	55039974	missense variant	G/A;T	snv	1.2E-02		6
rs17608766	LRRC37A2 ; GOSR2	1.000	0.040	17	46935905	3 prime UTR variant	T/C	snv		9.2E-02	6
rs4299376	LOC102725159 ; ABCG8	0.851	0.120	2	43845437	intron variant	G/C;T	snv			6
rs140570886	LPA	1.000	0.040	6	160591981	intron variant	T/C	snv		2.8E-02	3