DisGeNET - a database of gene-disease associations

List of associated variants

Carotid Artery Diseases, C0007273

Source: ALL

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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
rs2075650	TOMM40	0.662	0.360	19	44892362	intron variant	A/G	snv	0.13	0.13	45
rs646776	CELSR2	0.752	0.240	1	109275908	downstream gene variant	C/T	snv		0.74	25
rs1466535	LRP1	0.790	0.160	12	57140687	intron variant	G/A;C	snv			9
rs6065904	PLTP	1.000	0.080	20	45906012	intron variant	G/A	snv		0.23	7
rs3123629	LPAL2			6	160485054	intron variant	G/A	snv		0.28	2
rs1454626	VLDLR-AS1 ; VLDLR			9	2621030	intron variant	C/A	snv		0.66	1