DisGeNET - a database of gene-disease associations

List of shared variants

Diabetic Nephropathy, C0011881

Disease: Diabetes Mellitus

Source: ALL

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
rs7903146	TCF7L2	0.554	0.680	10	112998590	intron variant	C/G;T	snv			93
rs1049353	CNR1	0.630	0.600	6	88143916	synonymous variant	C/T	snv	0.21	0.20	42
rs1143770	MIRLET7A2 ; MIR100HG	0.882	0.200	11	122146890	intron variant	C/T	snv		0.53	4
rs11549465	HIF1A-AS3 ; HIF1A	0.597	0.680	14	61740839	missense variant	C/T	snv	8.8E-02	7.7E-02	55
rs11771443	NOS3	0.790	0.360	7	150990599	upstream gene variant	C/T	snv		0.16	8
rs1332629192	ALB	0.851	0.200	4	73404374	missense variant	C/T	snv			7
rs1416580204	MOK	0.608	0.720	14	102250837	missense variant	C/T	snv	4.0E-06	7.0E-06	49
rs2070600	AGER	0.561	0.760	6	32183666	missense variant	C/T	snv	5.3E-02	3.6E-02	82
rs2070744	NOS3	0.608	0.680	7	150992991	intron variant	C/T	snv		0.70	54
rs2243250	IL4	0.570	0.760	5	132673462	upstream gene variant	C/T	snv		0.35	61
rs290487	TCF7L2	0.776	0.280	10	113149972	intron variant	C/T	snv		0.16	10
rs4986791	TLR4	0.456	0.840	9	117713324	missense variant	C/T	snv	5.7E-02	4.9E-02	182
rs5443	CDCA3 ; GNB3	0.532	0.760	12	6845711	synonymous variant	C/T	snv	0.36	0.44	106
rs7222331	KRTAP3-3	0.925	0.120	17	40995605	upstream gene variant	C/T	snv		0.24	3
rs758130759	HNF1B	0.925	0.120	17	37699149	missense variant	C/T	snv	1.6E-05	1.4E-05	3
rs8192678	PPARGC1A	0.667	0.440	4	23814039	missense variant	C/T	snv	0.31	0.26	28
rs1137933	NOS2	0.882	0.160	17	27778906	synonymous variant	G/A	snv	0.20	0.21	4
rs17300539	ADIPOQ	0.752	0.320	3	186841671	upstream gene variant	G/A	snv		5.3E-02	11
rs1800562	LOC108783645 ; HFE	0.435	0.880	6	26092913	missense variant	G/A	snv	3.3E-02	3.8E-02	262
rs1800566	NQO1	0.576	0.680	16	69711242	missense variant	G/A	snv	0.25	0.21	59
rs1800629	TNF	0.472	0.920	6	31575254	upstream gene variant	G/A	snv	0.12	0.14	169
rs1801133	MTHFR	0.472	0.880	1	11796321	missense variant	G/A	snv	0.31	0.27	174
rs2228146	IL6R	0.925	0.120	1	154454574	missense variant	G/A	snv	1.3E-02; 4.0E-06	5.4E-02	3
rs2268388	ACACB	0.851	0.200	12	109205840	intron variant	G/A	snv		0.14	6
rs237025	SUMO4 ; TAB2	0.672	0.360	6	149400554	missense variant	G/A	snv	0.55	0.57	26