DisGeNET - a database of gene-disease associations

Source: GWASDB

Variants associated to the Disease: Serum total cholesterol 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
rs891142	CETP			16	56970065	intron variant	T/C	snv		0.97	1
rs9923854	CETP			16	56983090	intron variant	T/G	snv		0.10	2
rs9939224	CETP	1.000	0.040	16	56968820	intron variant	T/G	snv		0.75	6