DisGeNET - a database of gene-disease associations

List of shared variants

Ischemic stroke, C0948008

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
rs7493	PON2	0.677	0.440	7	95405463	missense variant	G/C	snv	0.27	0.27	24
rs854560	PON1	0.513	0.800	7	95316772	missense variant	A/C;G;N;T	snv	0.29		113
rs662	PON1	0.485	0.840	7	95308134	missense variant	T/C	snv	0.38	0.42	157
rs1324214	F3	0.925	0.120	1	94531732	intron variant	G/A	snv		0.21	3
rs3917639		0.925	0.120	1	94527220	downstream gene variant	C/T	snv			2
rs1045642	ABCB1	0.456	0.840	7	87509329	synonymous variant	A/G;T	snv	0.50		214
rs3825807	ADAMTS7	0.807	0.120	15	78796769	missense variant	A/G	snv	0.34	0.33	10
rs3812316	MLXIPL	0.763	0.240	7	73606007	missense variant	C/G	snv	0.10	9.4E-02	14
rs5443	CDCA3 ; GNB3	0.532	0.760	12	6845711	synonymous variant	C/T	snv	0.36	0.44	106
rs3200401	MASCRNA ; MALAT1 ; TALAM1	0.742	0.320	11	65504361	splice region variant	C/T	snv	0.17	0.17	11
rs281865545	PECAM1	0.695	0.360	17	64377836	missense variant	C/G;T	snv			18
rs1131012	PECAM1	0.763	0.280	17	64350416	missense variant	T/C	snv		0.38	10
rs1271572	ESR2	0.708	0.400	14	64295199	intron variant	A/C;T	snv			16
rs1256049	ESR2	0.645	0.560	14	64257333	synonymous variant	C/T	snv	6.7E-02	6.3E-02	32
rs1267969615	ACE	0.532	0.760	17	63490960	missense variant	T/C	snv	4.0E-06		100
rs5985	F13A1	0.724	0.280	6	6318562	missense variant	C/A;T	snv	0.20; 2.4E-05		20
rs3024477	F13A1	0.882	0.160	6	6250887	missense variant	T/A	snv	1.8E-02	1.9E-02	3
rs5982	F13A1	0.882	0.160	6	6174633	missense variant	G/A	snv	0.21	0.19	3
rs5882	CETP	0.649	0.400	16	56982180	missense variant	G/A;C	snv	0.62		35
rs708272	CETP	0.708	0.440	16	56962376	intron variant	G/A	snv	0.42	0.38	24
rs11591147	PCSK9	0.677	0.360	1	55039974	missense variant	G/A;T	snv	1.2E-02		28
rs11206510		0.763	0.240	1	55030366	intergenic variant	T/A;C;G	snv			16
rs11614913	HOXC6 ; MIR196A2	0.512	0.760	12	53991815	mature miRNA variant	C/T	snv	0.39	0.34	111
rs708495		0.925	0.120	14	52302622	intergenic variant	T/A	snv		0.57	3
rs5918	ITGB3	0.683	0.480	17	47283364	missense variant	T/C	snv	0.12	0.13	26