DisGeNET - a database of gene-disease associations

List of shared variants

Coronary Artery Disease, C1956346

Disease: Lipoprotein (a) measurement

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
rs7412	APOE	0.641	0.640	19	44908822	missense variant	C/T	snv	6.2E-02	7.9E-02	20
rs186696265		0.882	0.040	6	160690668	intergenic variant	C/T	snv		1.0E-02	6
rs140570886	LPA	1.000	0.040	6	160591981	intron variant	T/C	snv		2.8E-02	3
rs147555597	LPAL2	1.000	0.040	6	160490564	intron variant	G/A	snv		5.5E-03	2
rs41269133		1.000	0.040	6	160666831	intron variant	T/C	snv		8.8E-02	2
rs41272114	LPA	1.000	0.040	6	160585045	splice donor variant	C/A;T	snv	1.2E-05; 4.1E-02		2
rs4252185	PLG	1.000	0.040	6	160702419	intron variant	T/C	snv		5.7E-02	2
rs55730499	LPA	1.000	0.040	6	160584578	intron variant	C/T	snv		4.5E-02	2
rs6926458	LPA	1.000	0.040	6	160598834	intron variant	A/G;T	snv			2
rs73596816	LPA	1.000	0.040	6	160596331	intron variant	G/A	snv		3.6E-02	2
rs7770628	LPA	1.000	0.040	6	160597142	intron variant	C/T	snv		0.63	2