DisGeNET - a database of gene-disease associations

List of associated variants

Myocardial Ischemia, C0151744

Source: ALL

Results per page

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
rs11053646	OLR1	0.724	0.280	12	10160849	missense variant	C/G	snv	0.11	0.13	18
rs363050	SNAP25-AS1 ; SNAP25	0.790	0.240	20	10253609	intron variant	G/A	snv		0.57	8
rs5498	ICAM4 ; ICAM1	0.531	0.760	19	10285007	missense variant	A/G	snv	0.44	0.37	99
rs10903323	MSRA	0.807	0.160	8	10292057	intron variant	A/G	snv		0.15	8
rs2230808	ABCA1	0.827	0.240	9	104800523	missense variant	T/C	snv	0.71	0.60	6
rs33918808	ABCA1	1.000	0.040	9	104817351	missense variant	C/G;T	snv	3.5E-02; 4.0E-06		1
rs1239681664	ABCA1	0.716	0.320	9	104818690	synonymous variant	A/G	snv		7.0E-06	15
rs2066714	ABCA1	0.742	0.240	9	104824472	missense variant	T/C	snv	0.21	0.25	13
rs138880920	ABCA1	1.000	0.040	9	104826957	missense variant	C/G	snv	3.3E-03	1.8E-03	1
rs2066718	ABCA1	0.882	0.120	9	104826974	missense variant	C/G;T	snv	4.3E-04; 5.4E-02		7
rs6993770	ZFPM2 ; ZFPM2-AS1	0.925	0.080	8	105569300	intron variant	A/T	snv		0.31	9
rs4147929	ABCA7	0.882	0.120	19	1063444	intron variant	A/C;G	snv			3
rs567798234	AMPD2	0.851	0.120	1	109625326	missense variant	C/T	snv	4.1E-06	7.0E-06	5
rs752596535	LDLR	0.752	0.200	19	11105407	stop gained	C/A;G;T	snv	1.6E-05		14
rs544456198	LDLR	0.790	0.120	19	11116930	missense variant	G/T	snv	8.0E-06	2.8E-05	9
rs7903146	TCF7L2	0.554	0.680	10	112998590	intron variant	C/G;T	snv			93
rs4986791	TLR4	0.456	0.840	9	117713324	missense variant	C/T	snv	5.7E-02	4.9E-02	182
rs397507444	MTHFR	0.405	0.880	1	11794407	missense variant	T/G	snv			306
rs1217691063	MTHFR	0.330	0.920	1	11796309	missense variant	A/G	snv	4.0E-06	7.0E-06	614
rs3751143	P2RX7 ; LOC105370032	0.742	0.480	12	121184501	missense variant	A/C;G	snv	0.19; 4.0E-06		12
rs1801282	PPARG	0.500	0.840	3	12351626	missense variant	C/G	snv	0.11	8.9E-02	131
rs1144507	ZNF202	0.925	0.080	11	123729767	missense variant	A/C;G;T	snv	0.68		2
rs1805192	PPARG	0.510	0.840	3	12379739	missense variant	C/G	snv			121
rs2954029		0.807	0.160	8	125478730	intron variant	A/T	snv		0.42	14
rs4988235	MCM6	0.752	0.400	2	135851076	intron variant	G/A;C	snv			19