DisGeNET - a database of gene-disease associations

List of shared variants

Diabetes Mellitus, Non-Insulin-Dependent, C0011860

Disease: Metabolic Syndrome X

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
rs2267443	SREBF2	0.882	0.120	22	41891450	intron variant	A/G	snv		0.67	5
rs2270565	UCP1	0.882	0.080	4	140562317	missense variant	T/A	snv	8.9E-02	6.5E-02	4
rs2291725	GIP	0.882	0.120	17	48961770	missense variant	T/C	snv	0.50	0.40	4
rs340874	PROX1 ; PROX1-AS1	0.882	0.080	1	213985913	non coding transcript exon variant	T/C	snv		0.40	7
rs7202116	FTO	0.882	0.120	16	53787703	intron variant	A/G	snv		0.41	7
rs726344	FNDC5	0.882	0.120	1	32867503	intron variant	G/A	snv		0.16	3
rs7578326	LOC646736	0.882	0.080	2	226155937	TF binding site variant	A/G	snv		0.36	7
rs846910	HSD11B1 ; HSD11B1-AS1	0.882	0.160	1	209701909	intron variant	A/G	snv		0.95	6
rs925946	BDNF-AS	0.882	0.120	11	27645655	intron variant	T/G	snv		0.72	9
rs9465871	CDKAL1	0.882	0.120	6	20717024	intron variant	T/C	snv		0.30	4
rs10830962		0.851	0.160	11	92965261	upstream gene variant	C/A;G;T	snv			7
rs10938397		0.851	0.200	4	45180510	intergenic variant	A/G	snv		0.37	19
rs121912706	ANK2	0.851	0.200	4	113373306	missense variant	C/T	snv	1.0E-03	9.2E-04	5
rs146052672	HMGA1	0.851	0.160	6	34242693	intron variant	-/C	delins			5
rs17373080	NR1H2	0.851	0.160	19	50376267	5 prime UTR variant	C/G	snv		0.29	4
rs2144908	LOC105372629 ; HNF4A	0.851	0.120	20	44357077	intron variant	G/A	snv		0.18	5
rs2293855	MTMR9	0.851	0.120	8	11319901	non coding transcript exon variant	G/A	snv		0.35	5
rs3213445	CHKB-CPT1B ; CPT1B	0.851	0.120	22	50577409	missense variant	T/C	snv	0.12	8.9E-02	4
rs4641	LMNA	0.851	0.120	1	156137743	splice region variant	C/T	snv	0.26	0.21	6
rs5015480		0.851	0.120	10	92705802	downstream gene variant	C/T	snv		0.42	9
rs6923761	GLP1R	0.851	0.200	6	39066296	missense variant	G/A;C	snv	0.23; 4.0E-06		4
rs750359414	RETN	0.851	0.240	19	7669884	missense variant	C/G;T	snv	4.0E-06; 4.0E-06		5
rs9940128	FTO	0.851	0.120	16	53766842	intron variant	G/A	snv		0.42	10
rs10010131	WFS1	0.827	0.120	4	6291188	intron variant	A/G	snv	0.66	0.63	7
rs11646213		0.827	0.320	16	82609046	intergenic variant	A/T	snv		0.47	6