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 EXOME	AF GENOME	Num. diseases
rs10425738	CYP2G1P	19	40911822	non coding transcript exon variant	G/A	snv		0.74	2
rs73931391	LOC107985299 ; CYP2G1P	19	40901969	intron variant	A/G	snv		3.9E-02	2
rs72480748	CYP2G1P	19	40908576	non coding transcript exon variant	G/A	snv	0.31	0.27	1