DisGeNET - a database of gene-disease associations

List of associated variants

Dementia, Vascular, C0011269

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
rs699	AGT	0.501	0.800	1	230710048	missense variant	A/G	snv	0.55	0.58	134
rs7493	PON2	0.677	0.440	7	95405463	missense variant	G/C	snv	0.27	0.27	24
rs769665945	SERPINE1	0.882	0.160	7	101137079	missense variant	C/A;T	snv	4.0E-06; 3.6E-05		3
rs854560	PON1	0.513	0.800	7	95316772	missense variant	A/C;G;N;T	snv	0.29		113
rs893051	CLDN1	0.807	0.400	3	190321812	intron variant	G/A;C	snv			7
rs944050	ESR2	0.827	0.280	14	64233327	splice region variant	T/C	snv	9.5E-02	7.9E-02	5
rs951660	PHLDB2	1.000	0.120	3	111919285	intron variant	A/C	snv		0.86	1