DisGeNET - a database of gene-disease associations

List of shared variants

Atherosclerosis, C0004153

Disease: Diabetes

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
rs1298417395	COP1	0.882	0.080	1	176206716	missense variant	C/T	snv		1.4E-05	4
rs1440763451	PPARG	0.882	0.080	3	12416849	missense variant	A/G	snv	4.0E-06		4
rs4862423	ACSL1	0.882	0.080	4	184805394	intron variant	C/T	snv		0.37	4
rs755725121	PIK3CD	0.882	0.080	1	9716029	missense variant	G/A	snv	2.1E-05	7.0E-06	4
rs773297988	PIK3CB	0.882	0.080	3	138698965	missense variant	T/C	snv	4.0E-06	3.5E-05	4
rs774887459	SGSM3	0.882	0.080	22	40405776	missense variant	G/A	snv	4.0E-06		4
rs4076317	ANGPTL4	0.882	0.080	19	8364115	intron variant	C/G	snv		0.25	5
rs3861950	TNFSF4	0.827	0.160	1	173187153	intron variant	T/C	snv		0.47	7
rs4821480	MYH9	0.807	0.160	22	36299201	intron variant	G/T	snv		0.78	9
rs185847354	ADIPOQ ; ADIPOQ-AS1	0.763	0.160	3	186854460	missense variant	T/C	snv	3.1E-04	7.0E-05	11
rs20455	KIF6 ; LOC107986594	0.763	0.160	6	39357302	missense variant	A/G	snv	0.41	0.49	12
rs2536512	SOD3	0.752	0.280	4	24799693	missense variant	G/A;T	snv	0.55		14
rs5355	C1orf112 ; SELE	0.742	0.240	1	169726729	missense variant	G/A	snv	4.5E-02	3.3E-02	14
rs2295490	TRIB3	0.724	0.320	20	388261	missense variant	A/G;T	snv	0.18; 4.0E-06		16
rs3798220	LPA	0.732	0.160	6	160540105	missense variant	T/C	snv	5.6E-02	3.1E-02	16
rs1022113606	SOD3	0.732	0.280	4	24800161	missense variant	G/C	snv	1.6E-04	2.1E-05	17
rs1800777	CETP	0.724	0.280	16	56983407	missense variant	G/A	snv	3.7E-02	2.8E-02	17
rs2943641		0.763	0.160	2	226229029	intergenic variant	T/C	snv		0.67	18
rs10757274	CDKN2B-AS1	0.701	0.320	9	22096056	intron variant	A/G	snv		0.41	22
rs2229616	MC4R	0.732	0.200	18	60372043	missense variant	C/T	snv	1.6E-02	1.6E-02	22
rs375752214	NOS3	0.708	0.400	7	150998541	missense variant	C/T	snv	4.1E-06	4.2E-05	22
rs660339	UCP2	0.695	0.320	11	73978059	missense variant	G/A	snv	0.41	0.43	24
rs76863441	PLA2G7	0.672	0.440	6	46709361	missense variant	C/A	snv	4.5E-03	1.3E-03	25
rs1799895	SOD3	0.683	0.360	4	24800212	missense variant	C/G	snv	2.3E-02	1.2E-02	26
rs3135506	APOA5	0.708	0.400	11	116791691	missense variant	G/A;C	snv	3.0E-05; 6.8E-02		26