DisGeNET - a database of gene-disease associations

Source: ALL

Variants associated to the Gene: LINC02227 ×

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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
rs2149954	LINC02227	0.882	0.080	5	158393594	intron variant	C/T	snv		0.37	5
rs1952652	LINC02227			5	158384080	intron variant	A/T	snv		0.28	3
rs10051330	LINC02227			5	158392616	intron variant	A/G;T	snv			2
rs11960210	LINC02227			5	158390626	intron variant	T/C;G	snv			2
rs12716337	LINC02227			5	158387220	intron variant	T/A;C	snv			2
rs7701003	LINC02227			5	158397473	intron variant	A/G	snv		0.41	2
rs9313772	LINC02227			5	158377449	intron variant	C/T	snv		0.30	2
rs7719885	LINC02227			5	158389119	intron variant	A/G	snv		0.38	1