DisGeNET - a database of gene-disease associations

Source: GWASDB

Variants associated to the Disease: Coronary heart disease ×

Variants associated to the Gene: CETP ×

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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
rs1864163	CETP	0.882	0.120	16	56963321	intron variant	G/A	snv		0.26	8
rs1532624	CETP	0.851	0.160	16	56971567	intron variant	C/A	snv		0.34	7
rs1800775	CETP	0.790	0.240	16	56961324	upstream gene variant	C/A;G	snv	0.51; 5.7E-06		7
rs708272	CETP	0.708	0.440	16	56962376	intron variant	G/A	snv	0.42	0.38	4
rs2303790	CETP	0.724	0.280	16	56983380	missense variant	A/G	snv	2.6E-03	6.5E-04	3
rs4783961	CETP	0.851	0.320	16	56960982	upstream gene variant	G/A	snv	0.48	0.47	3
rs5882	CETP	0.649	0.400	16	56982180	missense variant	G/A;C	snv	0.62		3
rs1800777	CETP	0.724	0.280	16	56983407	missense variant	G/A	snv	3.7E-02	2.8E-02	2
rs5880	CETP	0.827	0.040	16	56981179	missense variant	G/C	snv	5.2E-02	3.7E-02	2