DisGeNET - a database of gene-disease associations

List of shared variants

Diabetes Mellitus, Non-Insulin-Dependent, C0011860

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 EXOME	AF GENOME	Num. diseases
rs11097432	PDLIM5	1.000	0.080	4	94658554	intron variant	T/C	snv		0.24	2
rs13306519	LEPR	1.000	0.080	1	65572246	intron variant	C/G;T	snv			2
rs2272592	DDAH2 ; CLIC1	1.000	0.080	6	31730575	5 prime UTR variant	T/C	snv		0.88	2
rs3762344	LOC105372879	1.000	0.080	1	206895327	upstream gene variant	G/A	snv		0.47	2
rs3864884	KCNQ1	1.000	0.080	11	2460862	intron variant	C/T	snv		0.30	2
rs75843691	EPHA4	1.000	0.080	2	221530901	intron variant	C/A;G;T	snv			2
rs7770619	PPARD	1.000	0.080	6	35382265	intron variant	C/T	snv		7.7E-02	2
rs12576239	KCNQ1	1.000	0.080	11	2481089	intron variant	C/T	snv		0.16	3
rs1372503923	ITGA2	0.925	0.160	5	53048731	missense variant	A/C	snv			3
rs1801273	FABP1	0.925	0.200	2	88126256	missense variant	C/T	snv	1.2E-05	2.1E-05	3
rs1805081	NPC1	0.925	0.120	18	23560468	missense variant	T/C	snv	0.33	0.29	3
rs76974938	CFAP298-TCP10L ; CFAP298	1.000	0.080	21	32609946	missense variant	C/T	snv	1.3E-04	5.5E-04	3
rs9817428	PPARG	0.925	0.120	3	12298768	intron variant	C/A	snv		0.31	3
rs1150256	IL24	0.925	0.120	1	206899788	intron variant	G/A	snv		0.40	4
rs11572080	CYP2C8	0.882	0.160	10	95067273	missense variant	C/A;T	snv	8.3E-02		4
rs2285666	ACE2	0.925	0.160	X	15592225	splice region variant	C/T	snv	6.2E-06; 0.28	0.23	4
rs4646188	ACE2	0.925	0.120	X	15583220	intron variant	A/G	snv		9.1E-02	4
rs9838915	KLF15	0.882	0.120	3	126347377	intron variant	G/A	snv		0.19	4
rs1037733674	GCG ; LOC101929532	0.882	0.120	2	162147429	missense variant	T/C	snv		1.4E-05	5
rs12500426	PDLIM5	0.851	0.240	4	94593458	intron variant	A/C	snv		0.54	5
rs146052672	HMGA1	0.851	0.160	6	34242693	intron variant	-/C	delins			5
rs183433761	GCG ; LOC101929532	0.851	0.200	2	162152278	5 prime UTR variant	T/C;G	snv			5
rs200487063	LEP	0.851	0.200	7	128241246	upstream gene variant	G/A	snv		2.1E-05	5
rs201739205	LOC108783654 ; HSD17B1	0.851	0.200	17	42552898	5 prime UTR variant	A/C	snv	7.8E-03	8.2E-03	5
rs223331	CISD2	0.851	0.160	4	102872408	intron variant	T/A;C	snv			5