DisGeNET - a database of gene-disease associations

Variant: rs1004982 ×

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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
rs1004982	LOC112268146 ; CYP19A1	0.925	0.080	15	51321614	non coding transcript exon variant	T/C;G	snv			2