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
rs769665945	SERPINE1	0.882	0.160	7	101137079	missense variant	C/A;T	snv	4.0E-06; 3.6E-05		3
rs1051266	SLC19A1	0.627	0.640	21	45537880	missense variant	T/C;G	snv	0.55; 4.4E-06		41
rs3813034	SLC6A4	0.827	0.160	17	30197786	3 prime UTR variant	A/C	snv		0.40	8
rs140701	SLC6A4	0.790	0.200	17	30211514	intron variant	C/T	snv		0.40	7
rs4795541	SLC6A4 ; LOC105371720	0.807	0.200	17	30237299	upstream gene variant	A/G	snv			7
rs290227	SYK	1.000	0.120	9	90874382	intron variant	G/A	snv		0.30	1
rs1800470	TGFB1	0.515	0.840	19	41353016	missense variant	G/A;C	snv	0.55; 2.4E-04		107