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
rs11646213		0.827	0.320	16	82609046	intergenic variant	A/T	snv		0.47	6
rs1275805226	AGT	0.776	0.240	1	230706148	frameshift variant	G/-	del		7.0E-06	12
rs1501299	ADIPOQ ; ADIPOQ-AS1	0.597	0.720	3	186853334	intron variant	G/C;T	snv			52
rs1567438	LPAL2	0.925	0.200	6	160458599	intron variant	T/C	snv		0.25	3
rs1799752	ACE	0.677	0.480	17	63488529	intron variant	-/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT	delins			25
rs1800764		0.790	0.320	17	63473168	upstream gene variant	C/G;T	snv			10
rs1800795	IL6-AS1 ; IL6 ; STEAP1B	0.494	0.840	7	22727026	intron variant	C/G	snv		0.71	140
rs1800796	IL6-AS1 ; STEAP1B ; IL6	0.555	0.760	7	22726627	non coding transcript exon variant	G/C	snv		9.9E-02	74
rs1805192	PPARG	0.510	0.840	3	12379739	missense variant	C/G	snv			121
rs2069837	IL6-AS1 ; IL6	0.724	0.520	7	22728408	intron variant	A/C;G	snv			18
rs2070744	NOS3	0.608	0.680	7	150992991	intron variant	C/T	snv		0.70	54
rs266729	ADIPOQ	0.637	0.560	3	186841685	upstream gene variant	C/A;G;T	snv			37
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
rs397507444	MTHFR	0.405	0.880	1	11794407	missense variant	T/G	snv			306
rs4293393	UMOD	0.827	0.200	16	20353266	intron variant	A/G	snv		0.20	8
rs4402960	IGF2BP2	0.724	0.400	3	185793899	intron variant	G/T	snv		0.38	21
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
rs7903146	TCF7L2	0.554	0.680	10	112998590	intron variant	C/G;T	snv			93
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
rs1217691063	MTHFR	0.330	0.920	1	11796309	missense variant	A/G	snv	4.0E-06	7.0E-06	614
rs1267969615	ACE	0.532	0.760	17	63490960	missense variant	T/C	snv	4.0E-06		100