DisGeNET - a database of gene-disease associations

Source: GWASCAT

Variants associated to the Disease: Body mass index ×

Variants associated to the Gene: LINC01122 ×

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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
rs929641	LINC01122			2	58565242	intron variant	A/G	snv		0.45	3
rs2075171	LINC01122			2	58461772	splice region variant	G/A	snv		0.18	2
rs10197655	LINC01122			2	58564285	intron variant	G/A;T	snv			1
rs13011109	LINC01122			2	58630284	intron variant	G/C	snv		0.39	1
rs1641155	LINC01122			2	58738076	intron variant	T/G	snv		0.33	1
rs1861412	LINC01122			2	58665930	intron variant	G/A	snv		0.48	1
rs4671328	LINC01122			2	58708147	intron variant	T/G	snv		0.56	1
rs7573672	LINC01122			2	58927970	intron variant	G/A;T	snv			1