DisGeNET - a database of gene-disease associations

Source: GWASDB

Variants associated to the Disease: High density lipoprotein measurement ×

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
rs820299	CETP			16	56966372	intron variant	G/A;C	snv			2
rs891144	CETP			16	56978024	non coding transcript exon variant	C/T	snv		7.3E-02	2
rs9923854	CETP			16	56983090	intron variant	T/G	snv		0.10	2
rs9930761	CETP			16	56973280	intron variant	T/C	snv	5.9E-02	7.3E-02	2
rs118146573	CETP			16	56967026	intron variant	G/A	snv		9.4E-02	1