DisGeNET - a database of gene-disease associations

List of shared variants

Coronary Artery Disease, C1956346

Disease: Systolic Pressure

Source: GWASCAT ×

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
rs10857147		1.000	0.040	4	80259918	intergenic variant	A/T	snv		0.25	9
rs111245230	SVEP1	1.000	0.040	9	110407495	missense variant	T/C	snv	2.6E-02	2.3E-02	3
rs11556924	ZC3HC1	0.752	0.240	7	130023656	missense variant	C/A;T	snv	4.0E-06; 0.28		13
rs1250259	FN1 ; LOC105373868	1.000	0.040	2	215435759	missense variant	T/A	snv	0.76	0.79	5
rs13139571	LOC107984032 ; GUCY1A1	1.000	0.040	4	155724361	intron variant	C/A	snv		0.22	7
rs1333049	CDKN2B-AS1	0.614	0.520	9	22125504	intron variant	G/C	snv		0.41	18
rs1378942	CSK	0.790	0.240	15	74785026	intron variant	C/A;T	snv			6
rs16948048	ZNF652 ; LOC102724596	0.925	0.040	17	49363104	intron variant	A/G	snv		0.37	5
rs17037390	MTHFR	1.000	0.040	1	11800786	non coding transcript exon variant	G/A	snv		0.18	3
rs17514846	FURIN	0.882	0.120	15	90873320	intron variant	C/A;G	snv			5
rs17608766	LRRC37A2 ; GOSR2	1.000	0.040	17	46935905	3 prime UTR variant	T/C	snv		9.2E-02	6
rs17696736	NAA25	0.827	0.240	12	112049014	intron variant	A/G	snv		0.30	12
rs2071382	FES	1.000	0.040	15	90884967	intron variant	T/C	snv		0.57	2
rs2107595		0.732	0.280	7	19009765	regulatory region variant	G/A	snv		0.19	8
rs2327429	TARID ; TCF21	0.882	0.120	6	133888699	non coding transcript exon variant	T/C	snv		0.24	2
rs2571445	TNS1	0.925	0.080	2	217818431	missense variant	A/G;T	snv	0.62		8
rs2681472	ATP2B1	0.882	0.080	12	89615182	intron variant	A/G	snv		0.14	6
rs2681492	ATP2B1	0.925	0.040	12	89619312	intron variant	T/C;G	snv			7
rs2972146		0.882	0.040	2	226235982	intergenic variant	G/T	snv		0.72	6
rs3184504	SH2B3 ; ATXN2	0.572	0.600	12	111446804	missense variant	T/A;C;G	snv	0.67		61
rs34991912	FGD5	1.000	0.040	3	14884844	intron variant	T/A;C	snv			2
rs3745348	MYO9B	1.000	0.040	19	17101600	intron variant	C/T	snv		0.38	2
rs3918226	NOS3	0.925	0.080	7	150993088	intron variant	C/T	snv		5.7E-02	9
rs4420638	APOC1	0.708	0.520	19	44919689	downstream gene variant	A/G	snv		0.18	30
rs604723	ARHGAP42	1.000	0.040	11	100739815	intron variant	T/C	snv		0.78	8