DisGeNET - a database of gene-disease associations

List of shared variants

Coronary Artery Disease, C1956346

Disease: Cardiovascular Diseases

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 GENOME	Num. diseases
rs10116277	CDKN2B-AS1	0.827	0.160	9	22081398	intron variant	G/T	snv	0.62	8
rs10455872	LPA	0.662	0.320	6	160589086	intron variant	A/G	snv	4.3E-02	33
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
rs10846744	SCARB1	0.763	0.160	12	124827879	intron variant	G/C	snv	0.32	11
rs10865710	PPARG	0.763	0.360	3	12311699	intron variant	C/G	snv	0.25	13
rs10903323	MSRA	0.807	0.160	8	10292057	intron variant	A/G	snv	0.15	8
rs10911021	LOC105371642 ; LINC01344	0.807	0.160	1	182112825	intron variant	C/T	snv	0.36	11
rs11066001	BRAP	0.763	0.360	12	111681367	intron variant	T/C	snv	5.8E-03	15
rs11206510		0.763	0.240	1	55030366	intergenic variant	T/A;C;G	snv		16
rs12740374	CELSR2	0.851	0.040	1	109274968	3 prime UTR variant	G/T	snv	0.22	16
rs12746200	PLA2G4A	0.851	0.160	1	186880054	intron variant	A/G	snv	7.3E-02	6
rs12785878	NADSYN1	0.677	0.520	11	71456403	intron variant	G/A;T	snv		25
rs1282382243	DLEU7-AS1 ; DLEU1 ; DLEU7	0.807	0.120	13	50843630	missense variant	G/A	snv		8
rs1333049	CDKN2B-AS1	0.614	0.520	9	22125504	intron variant	G/C	snv	0.41	60
rs140570886	LPA	1.000	0.040	6	160591981	intron variant	T/C	snv	2.8E-02	3
rs1501299	ADIPOQ ; ADIPOQ-AS1	0.597	0.720	3	186853334	intron variant	G/C;T	snv		52
rs1537375	CDKN2B-AS1	0.882	0.120	9	22116072	intron variant	T/C;G	snv		6
rs1544410	VDR	0.542	0.760	12	47846052	intron variant	C/A;G;T	snv		78
rs17321515		0.776	0.200	8	125474167	intron variant	A/G	snv	0.49	16
rs174546	FADS1 ; FADS2	0.807	0.200	11	61802358	3 prime UTR variant	C/T	snv	0.28	17
rs174547	FADS2 ; FADS1	0.742	0.240	11	61803311	intron variant	T/C	snv	0.28	33
rs17608766	LRRC37A2 ; GOSR2	1.000	0.040	17	46935905	3 prime UTR variant	T/C	snv	9.2E-02	8
rs1790349	DHCR7	0.882	0.040	11	71431304	intron variant	T/C	snv	0.19	4
rs1799752	ACE	0.677	0.480	17	63488529	intron variant	-/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT	delins		25