DisGeNET - a database of gene-disease associations

List of associated variants

Atherosclerosis, C0004153

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
rs445925	APOC1	0.882	0.080	19	44912383	non coding transcript exon variant	G/A;C	snv			10
rs879254850	MIR6886 ; LDLR	0.776	0.160	19	11113365	missense variant	A/G;T	snv	4.0E-06		9
rs4523	TBXA2R	0.776	0.280	19	3595796	missense variant	A/G	snv	0.56	0.66	8
rs879254925	MIR6886 ; LDLR	0.790	0.120	19	11113680	missense variant	G/T	snv			8
rs879254693	LDLR	0.807	0.160	19	11107424	missense variant	T/A;C;G	snv			7
rs121918393	APOE	0.851	0.120	19	44908756	missense variant	C/A;T	snv	1.3E-05; 9.0E-05		6
rs759003763	MIR6886 ; LDLR	0.827	0.120	19	11113585	missense variant	G/A	snv			6
rs1249040838	MIR6886 ; LDLR	0.827	0.120	19	11113699	missense variant	G/A	snv	4.0E-06		5
rs140808909	APOE	0.851	0.120	19	44909080	missense variant	G/A	snv	2.0E-04	5.6E-05	5
rs4076317	ANGPTL4	0.882	0.080	19	8364115	intron variant	C/G	snv		0.25	5
rs879254840	LDLR ; MIR6886	0.827	0.120	19	11113322	missense variant	A/G	snv			5
rs4987262	PTGIR	0.882	0.040	19	46623592	missense variant	G/A;C	snv	7.1E-03		4
rs879254582	LDLR	0.851	0.160	19	11105488	frameshift variant	AGCCCCT/-	delins			4
rs76992529	TTR	0.653	0.560	18	31598655	missense variant	G/A	snv	1.1E-03	4.9E-03	36
rs2229616	MC4R	0.732	0.200	18	60372043	missense variant	C/T	snv	1.6E-02	1.6E-02	22
rs1267969615	ACE	0.532	0.760	17	63490960	missense variant	T/C	snv	4.0E-06		100
rs5918	ITGB3	0.683	0.480	17	47283364	missense variant	T/C	snv	0.12	0.13	26
rs112735431	RNF213 ; RNF213-AS1	0.683	0.320	17	80385145	missense variant	G/A;C	snv	2.6E-04; 8.0E-06		24
rs281865545	PECAM1	0.695	0.360	17	64377836	missense variant	C/G;T	snv			18
rs7216389	GSDMB	0.732	0.440	17	39913696	intron variant	C/T	snv		0.60	14
rs2277680	CXCL16	0.776	0.160	17	4735268	missense variant	G/A	snv	0.47	0.41	10
rs12953	PECAM1	0.763	0.200	17	64356203	missense variant	C/A;T	snv		0.38	9
rs9303277	IKZF3	0.790	0.240	17	39820216	intron variant	C/T	snv		0.52	9
rs46522	UBE2Z	0.807	0.120	17	48911235	non coding transcript exon variant	C/T	snv		0.40	8
rs7217186	ALOX15	0.827	0.120	17	4636097	intron variant	C/T	snv		0.45	5