DisGeNET - a database of gene-disease associations

Source: GWASDB

Variants associated to the Disease: Serum total cholesterol measurement ×

Variants associated to the Gene: APP ×

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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
rs2829976	APP			21	25900162	intron variant	T/G	snv		3.6E-02	3
rs2829978	APP			21	25902056	intron variant	T/C	snv		2.9E-02	3
rs9984764	APP			21	26125180	intron variant	G/A	snv		1.1E-02	3