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
rs10118757	MTAP	0.827	0.120	9	21853340	intron variant	A/G	snv		0.26	7
rs10757274	CDKN2B-AS1	0.701	0.320	9	22096056	intron variant	A/G	snv		0.41	22
rs4977574	CDKN2B-AS1	0.695	0.520	9	22098575	intron variant	A/G;T	snv			26
rs2383206	CDKN2B-AS1	0.742	0.320	9	22115027	intron variant	A/G	snv		0.49	17
rs2383207	CDKN2B-AS1	0.695	0.280	9	22115960	intron variant	A/G	snv		0.64	22
rs1333045	CDKN2B-AS1	0.776	0.280	9	22119196	non coding transcript exon variant	T/C	snv		0.50	14
rs10757278	CDKN2B-AS1	0.620	0.520	9	22124478	intron variant	A/G	snv		0.40	44
rs1333049	CDKN2B-AS1	0.614	0.520	9	22125504	intron variant	G/C	snv		0.41	60
rs17465637	MIA3	0.790	0.200	1	222650187	intron variant	A/C;G;T	snv	0.64; 6.4E-06		11
rs1136410	PARP1	0.559	0.760	1	226367601	missense variant	A/G	snv	0.21	0.15	70
rs1800795	IL6-AS1 ; IL6 ; STEAP1B	0.494	0.840	7	22727026	intron variant	C/G	snv		0.71	140
rs1334899057	SSTR4	0.882	0.160	20	23035908	missense variant	T/C	snv		7.0E-06	4
rs2067853	AGT	0.851	0.160	1	230702512	downstream gene variant	G/A	snv		0.25	5
rs1177506410	AGT	0.776	0.240	1	230706148	missense variant	G/C	snv	4.0E-06	7.0E-06	12
rs1275805226	AGT	0.776	0.240	1	230706148	frameshift variant	G/-	del		7.0E-06	12
rs699	AGT	0.501	0.800	1	230710048	missense variant	A/G	snv	0.55	0.58	134
rs4762	AGT	0.637	0.440	1	230710231	missense variant	G/A	snv	0.12	0.11	35
rs3789679	AGT	0.925	0.120	1	230713948	intron variant	G/A;T	snv			4
rs5051	AGT	0.882	0.160	1	230714126	intron variant	C/A;G;T	snv			5
rs6742078	UGT1A3 ; UGT1A7 ; UGT1A8 ; UGT1A10 ; UGT1A6 ; UGT1A4 ; UGT1A9 ; UGT1A1 ; UGT1A5	0.807	0.240	2	233763993	intron variant	G/T	snv		0.36	13
rs1805087	MTR	0.496	0.800	1	236885200	missense variant	A/G	snv	0.20	0.21	135
rs1799945	LOC108783645 ; HFE	0.452	0.760	6	26090951	missense variant	C/G;T	snv	0.11	0.10	226
rs6929846	BTN2A1	0.827	0.160	6	26458037	5 prime UTR variant	T/C	snv		0.70	10
rs758801521	ADRA1A	0.882	0.160	8	26770618	missense variant	A/G	snv	4.0E-06		4