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	Chr	Position	Consequence	Alleles	Class	AF GENOME	Num. diseases
rs9408815	LINC01505	9	106128240	intron variant	C/G	snv	0.20	2
rs9409082	LINC01505	9	106138768	intron variant	C/T	snv	0.20	2
rs969650	LINC01505	9	106615799	non coding transcript exon variant	T/C	snv	0.49	1