DisGeNET - a database of gene-disease associations

Source: GWASDB

Variants associated to the Disease: Serum total cholesterol measurement ×

Variants associated to the Gene: SUGP1 ×

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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
rs10401969	SUGP1	0.776	0.240	19	19296909	intron variant	T/C	snv		0.10	6
rs1859287	SUGP1			19	19311378	intron variant	T/A;C;G	snv			4
rs2023883	SUGP1			19	19294671	intron variant	G/A	snv		0.19	4