DisGeNET - a database of gene-disease associations

Source: GWASCAT

Variants associated to the Gene: SENCR ×

Results per page

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
rs695113	FLI1 ; SENCR			11	128692203	intron variant	C/G;T	snv			1
rs10893909	SENCR ; FLI1			11	128695139	intron variant	C/T	snv		0.18	1