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
rs133029	PLA2G6	22	38180308	intron variant	C/T	snv	0.11	1
rs2277844	PLA2G6	22	38181508	intron variant	G/A	snv	0.53	1
rs5756931	PLA2G6	22	38150026	non coding transcript exon variant	T/A;C	snv		1