DisGeNET - a database of gene-disease associations

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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
rs117023642	LINC02153			8	20981609	intron variant	C/G	snv		1.6E-02	2
rs11788387				9	81855961	regulatory region variant	G/T	snv		0.14	2