DisGeNET - a database of gene-disease associations

List of shared variants

Cerebrovascular accident, C0038454

Disease: Coronary heart disease

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
rs11053646	OLR1	0.724	0.280	12	10160849	missense variant	C/G	snv	0.11	0.13	18
rs1416580204	MOK	0.608	0.720	14	102250837	missense variant	C/T	snv	4.0E-06	7.0E-06	49
rs13114738	SLC39A8	0.851	0.120	4	102363708	intron variant	C/A;T	snv			16
rs5498	ICAM4 ; ICAM1	0.531	0.760	19	10285007	missense variant	A/G	snv	0.44	0.37	99
rs146292819	ABCA1	0.790	0.240	9	104794495	missense variant	T/G	snv	2.9E-04	3.8E-04	9
rs2066718	ABCA1	0.882	0.120	9	104826974	missense variant	C/G;T	snv	4.3E-04; 5.4E-02		7
rs2230806	ABCA1	0.689	0.280	9	104858586	missense variant	C/T	snv	0.32	0.39	24
rs2288904	SLC44A2	0.807	0.240	19	10631494	missense variant	A/G	snv	0.80	0.83	8
rs9797861	SLC44A2	0.790	0.200	19	10632450	intron variant	C/A;G;T	snv			9
rs3900940	MYH15	0.827	0.040	3	108428881	missense variant	T/A;C	snv	4.3E-06; 0.24		6
rs2228315	SELPLG	0.807	0.120	12	108624122	missense variant	C/T	snv	0.11	0.14	7
rs629301	CELSR2	0.851	0.120	1	109275684	3 prime UTR variant	G/T	snv		0.74	22
rs599839	PSRC1	0.724	0.360	1	109279544	downstream gene variant	G/A;C	snv			27
rs1122608	SMARCA4	0.763	0.120	19	11052925	intron variant	G/T	snv		0.18	16
rs2200733		0.752	0.240	4	110789013	intergenic variant	C/T	snv		0.18	12
rs6533530		0.851	0.120	4	110810780	intergenic variant	T/C	snv		0.47	16
rs3184504	SH2B3 ; ATXN2	0.572	0.600	12	111446804	missense variant	T/A;C;G	snv	0.67		92
rs11065987		0.807	0.280	12	111634620	intergenic variant	A/G	snv		0.29	17
rs11066001	BRAP	0.763	0.360	12	111681367	intron variant	T/C	snv		5.8E-03	15
rs2339840	ALDH2	1.000	0.040	12	111817137	3 prime UTR variant	C/T	snv		3.4E-02	2
rs4506565	TCF7L2	0.790	0.280	10	112996282	intron variant	A/G;T	snv			22
rs7903146	TCF7L2	0.554	0.680	10	112998590	intron variant	C/G;T	snv			93
rs201058276	F7	0.776	0.240	13	113118731	missense variant	G/A;C	snv	4.8E-05; 4.0E-06		11
rs964184	ZPR1	0.716	0.440	11	116778201	3 prime UTR variant	G/C	snv		0.82	47
rs3135506	APOA5	0.708	0.400	11	116791691	missense variant	G/A;C	snv	3.0E-05; 6.8E-02		26