DisGeNET - a database of gene-disease associations

List of associated variants

Myocardial Infarction, C0027051

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
rs1048990	PSMA6	0.790	0.280	14	35292469	5 prime UTR variant	C/G;T	snv	0.19; 4.0E-06		8
rs1049636	FGG	1.000	0.080	4	154604818	3 prime UTR variant	G/A	snv	0.67	0.70	1
rs10507391	ALOX5AP	0.776	0.320	13	30737959	intron variant	A/T	snv		0.52	10
rs1050998	CXCL16	1.000	0.080	17	4735442	missense variant	A/G	snv	0.46	0.41	1
rs10518325	SEC24D	1.000	0.080	4	118796479	intron variant	A/G	snv		6.4E-02	1
rs1051931	PLA2G7	0.708	0.400	6	46705206	missense variant	A/G	snv	0.81	0.79	19
rs1052133	OGG1 ; CAMK1	0.476	0.800	3	9757089	missense variant	C/G	snv	0.27	0.22	147
rs1053874	DNASE1 ; TRAP1	0.851	0.240	16	3657746	missense variant	G/A;T	snv	0.36; 4.0E-06		7
rs1057335	SERPINF2	0.827	0.120	17	1754359	missense variant	G/A	snv	0.22	0.20	5
rs1058932	CYP2C8	1.000	0.080	10	95037104	3 prime UTR variant	G/A	snv	0.22	0.24	1
rs1061170	CFH	0.561	0.720	1	196690107	missense variant	C/T	snv	0.68	0.64	72
rs1063192	CDKN2B ; CDKN2B-AS1	0.695	0.520	9	22003368	3 prime UTR variant	G/A;T	snv			24
rs1063537	ADIPOQ-AS1 ; ADIPOQ	0.807	0.320	3	186856286	3 prime UTR variant	C/T	snv		9.6E-02	6
rs1063539	ADIPOQ ; ADIPOQ-AS1	0.827	0.360	3	186857603	3 prime UTR variant	G/A;C	snv		0.10	5
rs10733113		0.882	0.160	1	247459055	upstream gene variant	A/G	snv		0.81	3
rs10738605	CDKN2B-AS1	0.925	0.120	9	22049131	non coding transcript exon variant	C/A;G	snv			3
rs10738607	CDKN2B-AS1	0.925	0.080	9	22088095	intron variant	A/G	snv		0.42	4
rs10741657	CYP2R1	0.637	0.520	11	14893332	upstream gene variant	A/G	snv		0.65	34
rs10757274	CDKN2B-AS1	0.701	0.320	9	22096056	intron variant	A/G	snv		0.41	22
rs10757278	CDKN2B-AS1	0.620	0.520	9	22124478	intron variant	A/G	snv		0.40	44
rs10773989	ADIPOR2	0.925	0.160	12	1747816	intron variant	T/C	snv		0.41	5
rs10776909	RXRA	0.925	0.160	9	134396900	intron variant	T/C;G	snv			2
rs10788952	LRP8	1.000	0.080	1	53272428	non coding transcript exon variant	C/T	snv		0.37	1
rs10811650	CDKN2B-AS1	0.882	0.200	9	22067594	intron variant	A/G	snv		0.37	5
rs10811661		0.724	0.400	9	22134095	intergenic variant	T/C	snv		0.14	22