DisGeNET - a database of gene-disease associations

List of shared variants

Coronary Arteriosclerosis, C0010054

Disease: Hypertensive 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 GENOME	Num. diseases
rs10118757	MTAP	0.827	0.120	9	21853340	intron variant	A/G	snv	0.26	7
rs10741657	CYP2R1	0.637	0.520	11	14893332	upstream gene variant	A/G	snv	0.65	34
rs10754558	NLRP3	0.695	0.480	1	247448734	3 prime UTR variant	G/C;T	snv		20
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
rs11014166	CACNB2	0.882	0.040	10	18419869	intron variant	A/T	snv	0.27	10
rs1122608	SMARCA4	0.763	0.120	19	11052925	intron variant	G/T	snv	0.18	16
rs1333049	CDKN2B-AS1	0.614	0.520	9	22125504	intron variant	G/C	snv	0.41	60
rs1501299	ADIPOQ ; ADIPOQ-AS1	0.597	0.720	3	186853334	intron variant	G/C;T	snv		52
rs1761667	CD36	0.752	0.320	7	80615623	intron variant	G/A	snv	0.49	12
rs1799752	ACE	0.677	0.480	17	63488529	intron variant	-/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT	delins		25
rs1799998	CYP11B2	0.742	0.200	8	142918184	upstream gene variant	A/G;T	snv	0.38	14
rs180070	LINC01497	0.882	0.040	17	69960745	upstream gene variant	G/T	snv	0.77	4
rs1800795	IL6-AS1 ; IL6 ; STEAP1B	0.494	0.840	7	22727026	intron variant	C/G	snv	0.71	140
rs1805192	PPARG	0.510	0.840	3	12379739	missense variant	C/G	snv		121
rs2010963	VEGFA	0.542	0.840	6	43770613	5 prime UTR variant	C/G	snv	0.68	82
rs2070744	NOS3	0.608	0.680	7	150992991	intron variant	C/T	snv	0.70	54
rs2106261	ZFHX3	0.763	0.160	16	73017721	intron variant	C/G;T	snv		11
rs2144300	GALNT2	0.882	0.040	1	230159169	intron variant	C/T	snv	0.44	7
rs2275913	IL17A	0.514	0.760	6	52186235	upstream gene variant	G/A	snv	0.28	105
rs2282679	GC	0.645	0.480	4	71742666	intron variant	T/G	snv	0.21	38
rs2383207	CDKN2B-AS1	0.695	0.280	9	22115960	intron variant	A/G	snv	0.64	22
rs2576178	RNLS ; LIPJ	0.790	0.160	10	88583641	5 prime UTR variant	A/G	snv	0.29	9
rs266729	ADIPOQ	0.637	0.560	3	186841685	upstream gene variant	C/A;G;T	snv		37
rs3025058	MMP3	0.658	0.600	11	102845217	upstream gene variant	-/C;G	ins	2.8E-04	26