DisGeNET - a database of gene-disease associations

Source: GWASCAT

Variants associated to the Disease: Monocyte count result ×

Variants associated to the Gene: ACOXL ×

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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
rs150449635	ACOXL			2	110994574	intron variant	T/C	snv		1.5E-02	2
rs2062225	ACOXL			2	110993295	intron variant	A/C;T	snv			2
rs3789087	ACOXL ; MIR4435-2HG			2	111034076	intron variant	C/T	snv		0.14	2
rs3789088	ACOXL ; MIR4435-2HG			2	111033227	intron variant	G/C	snv		0.14	2
rs7578982	ACOXL ; MIR4435-2HG			2	111078961	intron variant	T/C	snv		0.27	2