DisGeNET - a database of gene-disease associations

List of shared variants

Hypertensive disease, C0020538

Disease: Myocardial Infarction

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
rs1213545562	TH	1.000	0.080	11	2166984	synonymous variant	G/A	snv	9.6E-06		2
rs12413409	CNNM2	0.790	0.200	10	102959339	intron variant	G/A	snv		9.0E-02	9
rs1384915680	TH	1.000	0.080	11	2166903	synonymous variant	G/A	snv	4.3E-06		2
rs148636776	ATXN2 ; SH2B3	0.790	0.280	12	111447491	missense variant	G/A	snv	1.5E-04	2.4E-04	18
rs1801133	MTHFR	0.472	0.880	1	11796321	missense variant	G/A	snv	0.31	0.27	174
rs197922	GOSR2 ; LRRC37A2	0.925	0.080	17	46931204	missense variant	G/A	snv	0.35	0.33	3
rs2067853	AGT	0.851	0.160	1	230702512	downstream gene variant	G/A	snv		0.25	5
rs243866	MMP2	0.827	0.120	16	55477625	intron variant	G/A	snv		0.19	8
rs367732974	F7	0.790	0.360	13	113105788	5 prime UTR variant	G/A	snv	8.9E-05	2.8E-05	9
rs4680	COMT ; MIR4761	0.442	0.920	22	19963748	missense variant	G/A	snv	0.46	0.44	249
rs4762	AGT	0.637	0.440	1	230710231	missense variant	G/A	snv	0.12	0.11	35
rs6313	HTR2A	0.562	0.640	13	46895805	synonymous variant	G/A	snv	0.41	0.40	82
rs662799	APOA5	0.689	0.480	11	116792991	upstream gene variant	G/A	snv		0.90	33
rs671	ALDH2	0.529	0.840	12	111803962	missense variant	G/A	snv	1.9E-02	5.8E-03	116
rs708272	CETP	0.708	0.440	16	56962376	intron variant	G/A	snv	0.42	0.38	24
rs72653706	ABCC6	0.695	0.480	16	16163078	stop gained	G/A	snv	1.4E-03	1.2E-03	32
rs755703581	PDX1	0.925	0.120	13	27920295	missense variant	G/A	snv	2.3E-05	7.0E-06	3
rs7913948	ALOX5	1.000	0.080	10	45373441	upstream gene variant	G/A	snv		0.17	3
rs17231896	CETP	0.925	0.120	16	56982180	missense variant	G/A;C	snv			3
rs1800470	TGFB1	0.515	0.840	19	41353016	missense variant	G/A;C	snv	0.55; 2.4E-04		107
rs1982073	TGFB1	0.649	0.640	19	41353016	missense variant	G/A;C	snv			32
rs3135506	APOA5	0.708	0.400	11	116791691	missense variant	G/A;C	snv	3.0E-05; 6.8E-02		26
rs4363	ACE	1.000	0.080	17	63497131	splice region variant	G/A;C	snv	0.52		2
rs5882	CETP	0.649	0.400	16	56982180	missense variant	G/A;C	snv	0.62		35
rs11575937	LMNA	0.653	0.480	1	156136985	missense variant	G/A;T	snv			29