DisGeNET - a database of gene-disease associations

List of shared variants

Obesity, C0028754

Disease: Coronary Artery Disease

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
rs1761667	CD36	0.752	0.320	7	80615623	intron variant	G/A	snv		0.49	12
rs20455	KIF6 ; LOC107986594	0.763	0.160	6	39357302	missense variant	A/G	snv	0.41	0.49	12
rs7895833		0.742	0.440	10	67863299	upstream gene variant	G/A;C	snv			12
rs10865710	PPARG	0.763	0.360	3	12311699	intron variant	C/G	snv		0.25	13
rs12970134		0.790	0.280	18	60217517	intergenic variant	G/A	snv		0.21	13
rs1803274	BCHE	0.763	0.360	3	165773492	missense variant	C/T	snv	0.18	0.18	13
rs2066714	ABCA1	0.742	0.240	9	104824472	missense variant	T/C	snv	0.21	0.25	13
rs670	APOA1 ; APOA1-AS	0.763	0.360	11	116837697	5 prime UTR variant	C/T	snv		0.17	13
rs7044343	LOC107987046 ; IL33	0.752	0.520	9	6254208	intron variant	C/T	snv		0.51	13
rs9282541	ABCA1	0.790	0.160	9	104858554	missense variant	G/A	snv	1.3E-02	4.4E-03	13
rs3812316	MLXIPL	0.763	0.240	7	73606007	missense variant	C/G	snv	0.10	9.4E-02	14
rs80356814	LMNA	0.732	0.320	1	156138697	synonymous variant	C/T	snv	8.0E-06		15
rs10767664	BDNF	0.752	0.400	11	27704439	intron variant	T/A	snv		0.83	16
rs116843064	ANGPTL4	0.776	0.160	19	8364439	missense variant	G/A	snv	1.3E-02	1.5E-02	16
rs1378942	CSK	0.790	0.240	15	74785026	intron variant	C/A;T	snv			16
rs1800588	ALDH1A2 ; LIPC	0.790	0.200	15	58431476	intron variant	C/G;T	snv	0.30		16
rs2016520	PPARD	0.752	0.320	6	35411001	5 prime UTR variant	C/T	snv		0.78	16
rs2237892	KCNQ1	0.790	0.320	11	2818521	intron variant	C/T	snv		9.2E-02	16
rs1801252	ADRB1	0.724	0.320	10	114044277	missense variant	A/G	snv	0.15	0.17	17
rs3819024	IL17A	0.701	0.560	6	52185988	upstream gene variant	A/G	snv		0.34	17
rs659366	UCP2	0.724	0.520	11	73983709	non coding transcript exon variant	C/T	snv		0.40	17
rs679620	MMP3	0.716	0.360	11	102842889	missense variant	T/C	snv	0.58	0.57	17
rs16147	LOC107986777 ; NPY	0.695	0.400	7	24283791	upstream gene variant	T/C	snv		0.48	18
rs2943641		0.763	0.160	2	226229029	intergenic variant	T/C	snv		0.67	18
rs182052	ADIPOQ	0.701	0.440	3	186842993	intron variant	G/A	snv		0.38	19