DisGeNET - a database of gene-disease associations

List of associated variants

Diabetes Mellitus, Non-Insulin-Dependent, C0011860

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
rs10401969	SUGP1	0.776	0.240	19	19296909	intron variant	T/C	snv		0.10	25
rs12785878	NADSYN1	0.677	0.520	11	71456403	intron variant	G/A;T	snv			25
rs4778889	IL16	0.683	0.480	15	81296654	intron variant	T/C	snv		0.24	24
rs6721961	NFE2L2	0.672	0.520	2	177265309	intron variant	T/C;G	snv		0.89	24
rs708272	CETP	0.708	0.440	16	56962376	intron variant	G/A	snv	0.42	0.38	24
rs10757274	CDKN2B-AS1	0.701	0.320	9	22096056	intron variant	A/G	snv		0.41	22
rs2383207	CDKN2B-AS1	0.695	0.280	9	22115960	intron variant	A/G	snv		0.64	22
rs4506565	TCF7L2	0.790	0.280	10	112996282	intron variant	A/G;T	snv			22
rs1558902	FTO	0.827	0.120	16	53769662	intron variant	T/A	snv		0.31	21
rs17817449	FTO	0.716	0.560	16	53779455	intron variant	T/A;G	snv			21
rs4402960	IGF2BP2	0.724	0.400	3	185793899	intron variant	G/T	snv		0.38	21
rs9651118	MTHFR	0.683	0.480	1	11802157	intron variant	T/C	snv		0.18	20
rs182052	ADIPOQ	0.701	0.440	3	186842993	intron variant	G/A	snv		0.38	19
rs4988235	MCM6	0.752	0.400	2	135851076	intron variant	G/A;C	snv			19
rs1121980	FTO	0.807	0.240	16	53775335	intron variant	G/A;C	snv			18
rs17251221	CASR	0.724	0.360	3	122274400	intron variant	A/G	snv		0.11	18
rs2074356	HECTD4	0.763	0.280	12	112207597	intron variant	G/A	snv		3.8E-03	18
rs560887	SPC25 ; G6PC2	0.827	0.120	2	168906638	intron variant	T/C	snv	0.79	0.80	18
rs687621	ABO	0.851	0.240	9	133261662	intron variant	G/A;C	snv			18
rs767649	MIR155HG ; MIR155	0.695	0.480	21	25572410	intron variant	T/A	snv		7.5E-02	18
rs2383206	CDKN2B-AS1	0.742	0.320	9	22115027	intron variant	A/G	snv		0.49	17
rs10767664	BDNF	0.752	0.400	11	27704439	intron variant	T/A	snv		0.83	16
rs174583	FADS2	0.807	0.320	11	61842278	intron variant	C/T	snv		0.35	16
rs2237892	KCNQ1	0.790	0.320	11	2818521	intron variant	C/T	snv		9.2E-02	16
rs822396	ADIPOQ	0.732	0.400	3	186849088	intron variant	G/A	snv		0.81	16