DisGeNET - a database of gene-disease associations

List of shared variants

Coronary Arteriosclerosis, C0010054

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
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
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
rs11542041	APOE	0.677	0.480	19	44908690	missense variant	C/A;T	snv	2.1E-05	23
rs12190287	TCF21	0.708	0.280	6	133893387	3 prime UTR variant	C/G;T	snv		19
rs1282382243	DLEU7-AS1 ; DLEU1 ; DLEU7	0.807	0.120	13	50843630	missense variant	G/A	snv		8
rs1333049	CDKN2B-AS1	0.614	0.520	9	22125504	intron variant	G/C	snv	0.41	60
rs1384889210	APOA1 ; APOA1-AS	0.827	0.040	11	116836193	missense variant	C/A	snv		5
rs16147	LOC107986777 ; NPY	0.695	0.400	7	24283791	upstream gene variant	T/C	snv	0.48	18
rs16933090	SOX6	0.790	0.160	11	16434247	5 prime UTR variant	C/T	snv	0.12	7
rs1746048		0.776	0.120	10	44280376	downstream gene variant	C/T	snv	0.25	8
rs1799889	SERPINE1	0.649	0.600	7	101126430	upstream gene variant	A/G	snv		31
rs1800795	IL6-AS1 ; IL6 ; STEAP1B	0.494	0.840	7	22727026	intron variant	C/G	snv	0.71	140
rs1800871	IL19 ; IL10	0.508	0.800	1	206773289	5 prime UTR variant	A/G	snv	0.69	108
rs1800872	IL19 ; IL10	0.495	0.840	1	206773062	5 prime UTR variant	T/G	snv	0.69	119
rs1805192	PPARG	0.510	0.840	3	12379739	missense variant	C/G	snv		121
rs20417	PACERR ; PTGS2	0.576	0.600	1	186681189	non coding transcript exon variant	C/G;T	snv		57
rs2106261	ZFHX3	0.763	0.160	16	73017721	intron variant	C/G;T	snv		11
rs2107595		0.732	0.280	7	19009765	regulatory region variant	G/A	snv	0.19	15
rs2227631	SERPINE1	0.742	0.200	7	101126257	upstream gene variant	A/G	snv	0.54	13
rs2453021	TNFRSF9	0.807	0.080	1	7929506	intron variant	C/A;T	snv		6
rs2518136	AHSG	0.851	0.120	3	186620038	intron variant	T/C	snv	0.46	4