DisGeNET - a database of gene-disease associations

List of shared variants

Coronary Artery Disease, C1956346

Disease: Diabetes Mellitus, Non-Insulin-Dependent

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
rs1081161		0.925	0.120	22	12200388	intergenic variant	G/A	snv			2
rs11112412	APPL2	0.925	0.120	12	105218537	intron variant	G/A	snv		0.18	2
rs13431554	IRS1	0.925	0.120	2	226732872	3 prime UTR variant	A/G	snv		0.10	2
rs2893880	ARID5B	0.925	0.120	10	61937857	intron variant	C/G;T	snv			2
rs3811951	LOC101929710 ; PCSK1	0.925	0.120	5	96426773	intron variant	A/G	snv		0.28	2
rs7756850	RAET1E ; RAET1E-AS1	0.925	0.120	6	149891460	intron variant	G/C	snv		0.40	2
rs9383921	RAET1E ; RAET1E-AS1	0.925	0.120	6	149889549	missense variant	C/T	snv	0.45	0.36	2
rs940494		0.925	0.120	7	56281231	intergenic variant	A/G	snv		0.20	2
rs1024610		0.882	0.200	17	34253212	upstream gene variant	T/A	snv		0.85	3
rs10761600	ARID5B	0.925	0.120	10	61997361	intron variant	A/G;T	snv			3
rs1254337	C14orf39	0.925	0.120	14	60453807	intron variant	A/T	snv		0.37	3
rs2297627	FOXO1	0.925	0.120	13	40659794	intron variant	A/G	snv		0.41	3
rs3737884	ADIPOR1	0.882	0.160	1	202944076	non coding transcript exon variant	C/T	snv		7.6E-02	3
rs7087507	ARID5B	0.925	0.120	10	61985930	intron variant	A/G	snv		0.33	3
rs9362054	LOC107986620 ; LINC01611	0.882	0.160	6	84468550	intron variant	T/C	snv		0.52	3
rs9371533	RAET1E-AS1 ; RAET1E	0.925	0.120	6	149889545	missense variant	G/A;C	snv	0.52		3
rs1150256	IL24	0.925	0.120	1	206899788	intron variant	G/A	snv		0.40	4
rs11572103	CYP2C8	0.851	0.120	10	95058349	missense variant	T/A	snv	1.6E-02	4.9E-02	4
rs2291725	GIP	0.882	0.120	17	48961770	missense variant	T/C	snv	0.50	0.40	4
rs3025035	VEGFA	0.851	0.240	6	43783622	non coding transcript exon variant	C/T	snv		0.14	4
rs663129		0.882	0.160	18	60171168	intergenic variant	G/A	snv		0.24	4
rs767870	ADIPOR2	0.882	0.120	12	1780657	intron variant	G/A;C	snv	0.82		4
rs805296	BAG6 ; APOM	0.851	0.120	6	31655116	intron variant	T/A;C	snv			4
rs10738610	CDKN2B-AS1	0.882	0.120	9	22123767	intron variant	A/C;T	snv			5
rs1205538057	ACE	0.827	0.200	17	63483937	missense variant	A/G	snv	4.0E-06		5