DisGeNET - a database of gene-disease associations

List of shared variants

Obesity, C0028754

Disease: Cardiovascular Diseases

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
rs10838738	MTCH2	1.000	0.080	11	47641497	intron variant	A/G	snv		0.28	6
rs11084753		1.000	0.080	19	33831232	intergenic variant	A/C;G;T	snv		0.65	6
rs35457250	AHSG	0.925	0.080	3	186620775	missense variant	C/T	snv	9.0E-03	8.1E-03	5
rs4638289	SAA1	1.000	0.080	11	18264227	upstream gene variant	A/T	snv		0.67	2
rs6731302	LINC01122	1.000	0.080	2	58606358	intron variant	A/G;T	snv			2
rs8179183	LEPR	1.000	0.080	1	65610269	missense variant	G/C;T	snv			3
rs4923461	BDNF-AS ; LINC00678	0.925	0.120	11	27635363	intron variant	A/C;G	snv			5
rs10911021	LOC105371642 ; LINC01344	0.807	0.160	1	182112825	intron variant	C/T	snv		0.36	11
rs116843064	ANGPTL4	0.776	0.160	19	8364439	missense variant	G/A	snv	1.3E-02	1.5E-02	16
rs1800437	GIPR	0.827	0.160	19	45678134	missense variant	G/C	snv	0.18	0.17	13
rs20455	KIF6 ; LOC107986594	0.763	0.160	6	39357302	missense variant	A/G	snv	0.41	0.49	12
rs3847987	VDR	0.882	0.160	12	47844285	3 prime UTR variant	C/A	snv		0.12	4
rs4149601	NEDD4L	0.882	0.160	18	58149559	splice region variant	G/A	snv	0.28	0.33	8
rs4917	AHSG	0.790	0.160	3	186619924	missense variant	T/C	snv	0.68	0.68	9
rs7968585	LINC02354	0.851	0.160	12	47838310	downstream gene variant	C/G;T	snv			7
rs10938397		0.851	0.200	4	45180510	intergenic variant	A/G	snv		0.37	19
rs2239179	VDR	0.790	0.200	12	47863983	intron variant	T/C	snv		0.39	9
rs9794	PPARD	0.882	0.200	6	35428018	3 prime UTR variant	G/A;C;T	snv			4
rs1044250	ANGPTL4	0.807	0.240	19	8371280	missense variant	C/T	snv	0.30	0.29	12
rs2237895	KCNQ1	0.790	0.240	11	2835964	intron variant	A/C;T	snv			10
rs3812316	MLXIPL	0.763	0.240	7	73606007	missense variant	C/G	snv	0.10	9.4E-02	14
rs2230806	ABCA1	0.689	0.280	9	104858586	missense variant	C/T	snv	0.32	0.39	24
rs3764261		0.732	0.280	16	56959412	upstream gene variant	C/A	snv		0.31	26
rs1801252	ADRB1	0.724	0.320	10	114044277	missense variant	A/G	snv	0.15	0.17	17
rs2016520	PPARD	0.752	0.320	6	35411001	5 prime UTR variant	C/T	snv		0.78	16