DisGeNET - a database of gene-disease associations

List of shared variants

Coronary heart disease, C0010068

Disease: Obesity

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
rs7649121	ADIPOQ	0.882	0.160	3	186850996	intron variant	A/T	snv		0.17	3
rs9300039		0.851	0.160	11	41893816	intergenic variant	C/A	snv		9.8E-02	4
rs12495941	ADIPOQ	0.851	0.280	3	186850391	intron variant	G/T	snv		0.35	5
rs142648132	MTR	0.827	0.160	1	236816521	missense variant	G/A;C;T	snv	8.4E-04; 2.4E-05		5
rs372359132	MTRR	0.827	0.160	5	7878203	missense variant	A/G	snv	4.0E-06	2.1E-05	5
rs3782889	MYL2	0.851	0.160	12	110912851	intron variant	A/G	snv		7.1E-02	5
rs3890182	ABCA1	0.925	0.120	9	104885374	intron variant	G/A;T	snv			5
rs939348	THRA	0.851	0.240	17	40075600	intron variant	T/C;G	snv			5
rs17366568	ADIPOQ ; ADIPOQ-AS1	0.851	0.200	3	186852664	non coding transcript exon variant	G/A	snv		8.8E-02	6
rs7901695	TCF7L2	0.851	0.160	10	112994329	intron variant	T/C	snv		0.34	6
rs10946398	CDKAL1	0.827	0.160	6	20660803	intron variant	A/C	snv		0.40	7
rs3846663	HMGCR ; CERT1	0.882	0.120	5	75359901	intron variant	C/T	snv		0.35	7
rs749710704	BHMT ; DMGDH	0.790	0.160	5	79119289	missense variant	C/G;T	snv	4.0E-06; 4.0E-06		7
rs7578597	THADA	0.807	0.240	2	43505684	missense variant	T/C	snv	9.9E-02	0.14	7
rs1467568	SIRT1	0.776	0.320	10	67915401	intron variant	A/G	snv		0.46	8
rs2297508	SREBF1	0.790	0.240	17	17812003	synonymous variant	C/G;T	snv	0.50; 7.5E-05		8
rs5082	APOA2	0.807	0.160	1	161223893	upstream gene variant	G/A	snv		0.68	8
rs4149313	ABCA1	0.763	0.240	9	104824472	missense variant	T/C	snv			9
rs4917	AHSG	0.790	0.160	3	186619924	missense variant	T/C	snv	0.68	0.68	9
rs1181860747	INSR	0.776	0.240	19	7122961	missense variant	C/T	snv			10
rs16998073		0.925	0.120	4	80263187	upstream gene variant	A/G;T	snv			10
rs3774261	ADIPOQ ; ADIPOQ-AS1	0.776	0.320	3	186853770	splice region variant	A/G	snv		0.55	10
rs10911021	LOC105371642 ; LINC01344	0.807	0.160	1	182112825	intron variant	C/T	snv		0.36	11
rs1320702652	MFAP1	0.752	0.160	15	43824536	missense variant	G/A	snv	4.0E-06		11
rs1799941	SHBG	0.763	0.280	17	7630105	5 prime UTR variant	G/A	snv		0.18	11