DisGeNET - a database of gene-disease associations

List of shared variants

Diabetic Nephropathy, C0011881

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
rs11538209	ALB	1.000	0.120	4	73404356	missense variant	T/C	snv			2
rs1567438	LPAL2	0.925	0.200	6	160458599	intron variant	T/C	snv		0.25	3
rs4293393	UMOD	0.827	0.200	16	20353266	intron variant	A/G	snv		0.20	8
rs5030718	TLR4	0.827	0.200	9	117713548	stop gained	G/A;T	snv	3.1E-03; 8.0E-06		8
rs11643718	SLC12A3	0.807	0.240	16	56899607	missense variant	G/A	snv	0.11	8.4E-02	10
rs1177506410	AGT	0.776	0.240	1	230706148	missense variant	G/C	snv	4.0E-06	7.0E-06	12
rs1275805226	AGT	0.776	0.240	1	230706148	frameshift variant	G/-	del		7.0E-06	12
rs1800775	CETP	0.790	0.240	16	56961324	upstream gene variant	C/A;G	snv	0.51; 5.7E-06		18
rs5030717	TLR4	0.807	0.240	9	117711556	intron variant	A/G	snv		0.13	9
rs7756992	CDKAL1	0.827	0.240	6	20679478	intron variant	A/G;T	snv			12
rs805304	CLIC1 ; DDAH2	0.851	0.240	6	31730311	5 prime UTR variant	T/G	snv		0.48	5
rs852426	ACTB	0.882	0.240	7	5526722	downstream gene variant	C/T	snv		0.39	5
rs281432	ICAM1	0.851	0.280	19	10279982	intron variant	C/G	snv		0.52	12
rs3918188	NOS3	0.776	0.280	7	151005693	intron variant	C/A;T	snv			10
rs11646213		0.827	0.320	16	82609046	intergenic variant	A/T	snv		0.47	6
rs1800764		0.790	0.320	17	63473168	upstream gene variant	C/G;T	snv			10
rs316019	SLC22A2	0.790	0.360	6	160249250	missense variant	A/C	snv	0.90	0.89	8
rs3742264	CPB2 ; CPB2-AS1	0.742	0.400	13	46073959	missense variant	C/T	snv	0.31	0.35	17
rs4402960	IGF2BP2	0.724	0.400	3	185793899	intron variant	G/T	snv		0.38	21
rs688	LDLR	0.742	0.400	19	11116926	synonymous variant	C/T	snv	0.39	0.34	16
rs751141	EPHX2	0.732	0.400	8	27516348	missense variant	G/A	snv	0.12	0.10	16
rs4762	AGT	0.637	0.440	1	230710231	missense variant	G/A	snv	0.12	0.11	35
rs8192678	PPARGC1A	0.667	0.440	4	23814039	missense variant	C/T	snv	0.31	0.26	28
rs1799752	ACE	0.677	0.480	17	63488529	intron variant	-/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT	delins			25
rs2069837	IL6-AS1 ; IL6	0.724	0.520	7	22728408	intron variant	A/C;G	snv			18