DisGeNET - a database of gene-disease associations

Source: GWASCAT

Variants associated to the Disease: Eosinophil count procedure ×

Variants associated to the Gene: CHD7 ×

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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
rs7846314	CHD7			8	60738272	intron variant	A/T	snv		0.27	5
rs35914442	CHD7			8	60724328	intron variant	A/G	snv		0.17	2
rs4449834	CHD7			8	60843309	intron variant	G/T	snv		0.71	2
rs13277976	CHD7			8	60766479	intron variant	A/T	snv		0.77	1
rs6994642	CHD7			8	60811218	intron variant	C/T	snv		0.18	1
rs7842389	CHD7			8	60772635	intron variant	C/T	snv		0.77	1