DisGeNET - a database of gene-disease associations

List of shared variants

Diabetes Mellitus, Non-Insulin-Dependent, C0011860

Disease: Diabetes Mellitus, Insulin-Dependent

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
rs1358030		0.925	0.120	10	106363841	intergenic variant	G/A	snv		0.57	2
rs1801262	NEUROD1 ; CERKL	0.882	0.120	2	181678728	missense variant	T/C	snv	0.70	0.68	4
rs560887	SPC25 ; G6PC2	0.827	0.120	2	168906638	intron variant	T/C	snv	0.79	0.80	18
rs7111341		0.925	0.120	11	2191936	regulatory region variant	C/T	snv		0.29	2
rs777334819	PPARG	0.925	0.120	3	12379856	missense variant	G/A	snv	3.6E-05	2.1E-05	2
rs8192556	NEUROD1 ; CERKL	0.925	0.120	2	181678271	missense variant	G/T	snv	1.9E-02	1.6E-02	2
rs9273368	HLA-DQB1-AS1	0.882	0.120	6	32658698	upstream gene variant	G/A	snv		0.23	3
rs1131580	TNFSF10	0.882	0.160	3	172505830	3 prime UTR variant	A/C;G;T	snv			4
rs1801483	GCGR	0.851	0.160	17	81809839	missense variant	G/A	snv	7.4E-03	6.3E-03	7
rs7202877		0.882	0.160	16	75213347	intergenic variant	T/C;G	snv			3
rs769985775	DMD	0.851	0.160	X	32448630	synonymous variant	T/C	snv	5.7E-06	9.5E-06	6
rs1205538057	ACE	0.827	0.200	17	63483937	missense variant	A/G	snv	4.0E-06		5
rs1332629192	ALB	0.851	0.200	4	73404374	missense variant	C/T	snv			7
rs2260000	PRRC2A	0.851	0.200	6	31625699	intron variant	A/G	snv		0.29	7
rs5435	SLC2A4	0.851	0.200	17	7283804	missense variant	T/A;C	snv	0.65		6
rs10758593	GLIS3	0.827	0.240	9	4292083	intron variant	G/A	snv		0.45	8
rs11154178	LOC105377982 ; TRDN	0.807	0.240	6	123540174	intron variant	T/A;C	snv			7
rs1121980	FTO	0.807	0.240	16	53775335	intron variant	G/A;C	snv			18
rs28485846	UNC5D	0.807	0.240	8	35265058	intron variant	C/T	snv		5.1E-02	7
rs3761980	MAPK14 ; SLC26A8	0.807	0.240	6	36026129	upstream gene variant	A/G	snv		0.14	7
rs4866	NUDT1	0.827	0.240	7	2249951	missense variant	G/A	snv	2.2E-02	1.8E-02	5
rs71597855		0.807	0.240	4	53790270	intron variant	G/A	snv		2.5E-02	7
rs734312	WFS1	0.790	0.240	4	6301627	missense variant	G/A	snv	0.55	0.42	10
rs762890235	ACE2	0.827	0.240	X	15578220	missense variant	G/T	snv	3.8E-05	9.5E-06	5
rs80028505	MAPK14	0.807	0.240	6	36030611	intron variant	C/G;T	snv			7