DisGeNET - a database of gene-disease associations

List of shared variants

Atherosclerosis, C0004153

Disease: Arteriosclerosis

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 GENOME	Num. diseases
rs1008438	HSPA1L ; HSPA1A	0.807	0.120	6	31815431	upstream gene variant	A/C;T	snv		6
rs1010	VAMP8	0.807	0.120	2	85581859	3 prime UTR variant	T/C;G	snv		7
rs10455872	LPA	0.662	0.320	6	160589086	intron variant	A/G	snv	4.3E-02	33
rs1056515	RGS5	0.882	0.040	1	163143470	3 prime UTR variant	G/T	snv	0.37	3
rs10757274	CDKN2B-AS1	0.701	0.320	9	22096056	intron variant	A/G	snv	0.41	22
rs10757278	CDKN2B-AS1	0.620	0.520	9	22124478	intron variant	A/G	snv	0.40	44
rs10846744	SCARB1	0.763	0.160	12	124827879	intron variant	G/C	snv	0.32	11
rs1122608	SMARCA4	0.763	0.120	19	11052925	intron variant	G/T	snv	0.18	16
rs1130864	CRP	0.672	0.520	1	159713301	3 prime UTR variant	G/A	snv	0.26	27
rs11542041	APOE	0.677	0.480	19	44908690	missense variant	C/A;T	snv	2.1E-05	23
rs1205	CRP	0.602	0.680	1	159712443	3 prime UTR variant	C/T	snv	0.30	46
rs12190287	TCF21	0.708	0.280	6	133893387	3 prime UTR variant	C/G;T	snv		19
rs12564445	TNNT2	0.851	0.040	1	201376359	intron variant	G/A	snv	0.27	5
rs12762303	ALOX5	0.851	0.080	10	45373723	upstream gene variant	T/C	snv	0.17	4
rs1282382243	DLEU7-AS1 ; DLEU1 ; DLEU7	0.807	0.120	13	50843630	missense variant	G/A	snv		8
rs12953	PECAM1	0.763	0.200	17	64356203	missense variant	C/A;T	snv	0.38	9
rs1298417395	COP1	0.882	0.080	1	176206716	missense variant	C/T	snv	1.4E-05	4
rs1314386070	DECR1	0.827	0.240	8	90042766	missense variant	T/C	snv	1.4E-05	9
rs1333049	CDKN2B-AS1	0.614	0.520	9	22125504	intron variant	G/C	snv	0.41	60
rs13447720	MRE11	0.925	0.040	11	94432160	intron variant	T/C	snv	0.17	2
rs1378942	CSK	0.790	0.240	15	74785026	intron variant	C/A;T	snv		16
rs1384889210	APOA1 ; APOA1-AS	0.827	0.040	11	116836193	missense variant	C/A	snv		5
rs1403934301	SHBG	0.882	0.120	17	7631317	missense variant	G/A	snv		3
rs1447295	CASC8	0.658	0.400	8	127472793	intron variant	A/C;T	snv		29
rs145204276	ZBTB37 ; SNORD74 ; SNORD75 ; GAS5 ; SNORD77 ; SNORA103 ; SNORD76	0.658	0.320	1	173868254	splice donor variant	CAAGG/-	delins	8.8E-02	31