DisGeNET - a database of gene-disease associations

List of associated variants

Myocardial Infarction, C0027051

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
rs3184504	SH2B3 ; ATXN2	0.572	0.600	12	111446804	missense variant	T/A;C;G	snv	0.67		92
rs148636776	ATXN2 ; SH2B3	0.790	0.280	12	111447491	missense variant	G/A	snv	1.5E-04	2.4E-04	18
rs653178	ATXN2	0.672	0.600	12	111569952	intron variant	C/T	snv		0.67	41
rs33980500	TRAF3IP2-AS1 ; TRAF3IP2	0.742	0.200	6	111592059	missense variant	C/T	snv	8.6E-02	9.7E-02	14
rs3782886	BRAP	0.724	0.480	12	111672685	synonymous variant	T/C	snv	1.9E-02	5.9E-03	22
rs11066001	BRAP	0.763	0.360	12	111681367	intron variant	T/C	snv		5.8E-03	15
rs671	ALDH2	0.529	0.840	12	111803962	missense variant	G/A	snv	1.9E-02	5.8E-03	116
rs1143634	IL1B	0.597	0.680	2	112832813	synonymous variant	G/A	snv	0.19	0.19	52
rs16944	IL1B	0.531	0.920	2	112837290	upstream gene variant	A/G	snv		0.57	92
rs367732974	F7	0.790	0.360	13	113105788	5 prime UTR variant	G/A	snv	8.9E-05	2.8E-05	9
rs201058276	F7	0.776	0.240	13	113118731	missense variant	G/A;C	snv	4.8E-05; 4.0E-06		11
rs6046	F7	0.925	0.080	13	113118845	missense variant	G/A;C;T	snv	0.13		5
rs537765533	IL1RN	0.882	0.080	2	113132839	missense variant	G/C	snv	2.0E-05		3
rs374100662	PRB2 ; PRB1	1.000	0.080	12	11393060	missense variant	G/A	snv			1
rs6318	HTR2C ; LOC105373313	0.623	0.520	X	114731326	missense variant	C/G;T	snv			42
rs4804611	ZNF627	0.925	0.080	19	11617987	3 prime UTR variant	A/G	snv		0.24	2
rs2075291	APOA5 ; ZPR1	0.752	0.400	11	116790676	missense variant	C/A;T	snv	6.4E-03; 4.0E-06		15
rs3135507	ZPR1 ; APOA5	0.925	0.120	11	116790772	missense variant	C/T	snv	5.0E-02	5.5E-02	3
rs3135506	APOA5	0.708	0.400	11	116791691	missense variant	G/A;C	snv	3.0E-05; 6.8E-02		26
rs662799	APOA5	0.689	0.480	11	116792991	upstream gene variant	G/A	snv		0.90	33
rs369066087	APOA1-AS ; APOA1	1.000	0.080	11	116837117	synonymous variant	G/A;C	snv	2.0E-05	2.8E-05	1
rs619203	ROS1	0.851	0.160	6	117301021	missense variant	G/C	snv	0.20	0.19	6
rs529038	ROS1	0.827	0.120	6	117301070	missense variant	C/G;T	snv	0.20	0.19	6
rs1927911	TLR4	0.658	0.640	9	117707776	intron variant	A/G	snv		0.62	28
rs4986790	TLR4	0.438	0.800	9	117713024	missense variant	A/G;T	snv	6.1E-02; 4.0E-06		223