DisGeNET - a database of gene-disease associations

List of shared variants

Diabetes Mellitus, Non-Insulin-Dependent, C0011860

Disease: Diabetes Mellitus

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
rs2070600	AGER	0.561	0.760	6	32183666	missense variant	C/T	snv	5.3E-02	3.6E-02	82
rs4762	AGT	0.637	0.440	1	230710231	missense variant	G/A	snv	0.12	0.11	35
rs699	AGT	0.501	0.800	1	230710048	missense variant	A/G	snv	0.55	0.58	134
rs5186	AGTR1	0.630	0.560	3	148742201	3 prime UTR variant	A/C	snv	0.23	0.21	38
rs4917	AHSG	0.790	0.160	3	186619924	missense variant	T/C	snv	0.68	0.68	9
rs759853	AKR1B1	0.827	0.320	7	134459206	non coding transcript exon variant	G/A	snv		0.33	6
rs1332629192	ALB	0.851	0.200	4	73404374	missense variant	C/T	snv			7
rs671	ALDH2	0.529	0.840	12	111803962	missense variant	G/A	snv	1.9E-02	5.8E-03	116
rs1044250	ANGPTL4	0.807	0.240	19	8371280	missense variant	C/T	snv	0.30	0.29	12
rs2278426	ANGPTL8 ; DOCK6	1.000	0.080	19	11239812	missense variant	C/T	snv	0.11	0.11	11
rs892066	ANGPTL8 ; DOCK6	1.000	0.080	19	11239664	synonymous variant	C/G	snv	0.22	0.33	2
rs2476601	AP4B1-AS1 ; PTPN22	0.498	0.800	1	113834946	missense variant	A/G	snv	0.93	0.93	121
rs2281068	APLN	0.925	0.080	X	129653796	intron variant	T/C	snv		0.31	3
rs5082	APOA2	0.807	0.160	1	161223893	upstream gene variant	G/A	snv		0.68	8
rs3135506	APOA5	0.708	0.400	11	116791691	missense variant	G/A;C	snv	3.0E-05; 6.8E-02		26
rs662799	APOA5	0.689	0.480	11	116792991	upstream gene variant	G/A	snv		0.90	33
rs4420638	APOC1	0.708	0.520	19	44919689	downstream gene variant	A/G	snv		0.18	43
rs2276415	AQP11 ; CLNS1A	0.882	0.160	11	77590296	missense variant	G/A	snv	0.14	0.13	6
rs4838605	ARHGAP22	0.882	0.160	10	48491914	intron variant	C/T	snv		0.38	4
rs10761600	ARID5B	0.925	0.120	10	61997361	intron variant	A/G;T	snv			3
rs2070150	ATF6	0.827	0.280	1	161791486	missense variant	G/C	snv	0.14	9.2E-02	6
rs189037	ATM ; NPAT	0.689	0.400	11	108223106	5 prime UTR variant	G/A	snv		0.49	22
rs1803274	BCHE	0.763	0.360	3	165773492	missense variant	C/T	snv	0.18	0.18	13
rs10767664	BDNF	0.752	0.400	11	27704439	intron variant	T/A	snv		0.83	16
rs759834365	BDNF-AS ; BDNF	0.448	0.760	11	27658456	missense variant	C/T	snv	1.2E-05		237