DisGeNET - a database of gene-disease associations

List of shared variants

Hypertensive disease, C0020538

Disease: Diabetes Mellitus, Non-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
rs11097432	PDLIM5	1.000	0.080	4	94658554	intron variant	T/C	snv		0.24	2
rs12576239	KCNQ1	1.000	0.080	11	2481089	intron variant	C/T	snv		0.16	3
rs13306519	LEPR	1.000	0.080	1	65572246	intron variant	C/G;T	snv			2
rs2272592	DDAH2 ; CLIC1	1.000	0.080	6	31730575	5 prime UTR variant	T/C	snv		0.88	2
rs3762344	LOC105372879	1.000	0.080	1	206895327	upstream gene variant	G/A	snv		0.47	2
rs3864884	KCNQ1	1.000	0.080	11	2460862	intron variant	C/T	snv		0.30	2
rs75843691	EPHA4	1.000	0.080	2	221530901	intron variant	C/A;G;T	snv			2
rs76974938	CFAP298-TCP10L ; CFAP298	1.000	0.080	21	32609946	missense variant	C/T	snv	1.3E-04	5.5E-04	3
rs7770619	PPARD	1.000	0.080	6	35382265	intron variant	C/T	snv		7.7E-02	2
rs10224002	PRKAG2	0.925	0.080	7	151717955	intron variant	A/G	snv		0.31	12
rs1150256	IL24	0.925	0.120	1	206899788	intron variant	G/A	snv		0.40	4
rs1372503923	ITGA2	0.925	0.160	5	53048731	missense variant	A/C	snv			3
rs1801273	FABP1	0.925	0.200	2	88126256	missense variant	C/T	snv	1.2E-05	2.1E-05	3
rs1805081	NPC1	0.925	0.120	18	23560468	missense variant	T/C	snv	0.33	0.29	3
rs2285666	ACE2	0.925	0.160	X	15592225	splice region variant	C/T	snv	6.2E-06; 0.28	0.23	4
rs2393791	HNF1A	0.925	0.160	12	120986153	intron variant	C/T	snv		0.62	8
rs4646188	ACE2	0.925	0.120	X	15583220	intron variant	A/G	snv		9.1E-02	4
rs7310409	HNF1A	0.925	0.160	12	120987058	intron variant	A/C;G;T	snv			7
rs9817428	PPARG	0.925	0.120	3	12298768	intron variant	C/A	snv		0.31	3
rs1037733674	GCG ; LOC101929532	0.882	0.120	2	162147429	missense variant	T/C	snv		1.4E-05	5
rs11572080	CYP2C8	0.882	0.160	10	95067273	missense variant	C/A;T	snv	8.3E-02		4
rs225015	DIO2	0.882	0.160	14	80201236	3 prime UTR variant	G/A	snv		0.37	5
rs2259820	HNF1A	0.882	0.160	12	120997539	synonymous variant	C/T	snv	0.34	0.26	6
rs846910	HSD11B1 ; HSD11B1-AS1	0.882	0.160	1	209701909	intron variant	A/G	snv		0.95	6
rs852426	ACTB	0.882	0.240	7	5526722	downstream gene variant	C/T	snv		0.39	5