DisGeNET - a database of gene-disease associations

List of shared variants

Hypertensive disease, C0020538

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
rs2282679	GC	0.645	0.480	4	71742666	intron variant	T/G	snv		0.21	38
rs26802	GHRLOS ; GHRL	0.925	0.160	3	10290681	intron variant	T/G	snv		0.31	3
rs397507444	MTHFR	0.405	0.880	1	11794407	missense variant	T/G	snv			306
rs753152	RAMP2-AS1 ; RAMP2	0.882	0.160	17	42761487	intron variant	T/G	snv		0.12	6
rs805304	CLIC1 ; DDAH2	0.851	0.240	6	31730311	5 prime UTR variant	T/G	snv		0.48	5
rs1801058	GRK4	0.882	0.120	4	3037423	missense variant	T/C;G	snv	0.62		4
rs183433761	GCG ; LOC101929532	0.851	0.200	2	162152278	5 prime UTR variant	T/C;G	snv			5
rs2241766	ADIPOQ ; ADIPOQ-AS1	0.608	0.720	3	186853103	synonymous variant	T/C;G	snv	8.0E-06; 0.13		48
rs5351	EDNRB-AS1 ; EDNRB	0.807	0.240	13	77901178	synonymous variant	T/C;G	snv	0.57		7
rs939348	THRA	0.851	0.240	17	40075600	intron variant	T/C;G	snv			5
rs12490383	SCAP	1.000	0.080	3	47452667	intron variant	T/C	snv		0.14	2
rs1267969615	ACE	0.532	0.760	17	63490960	missense variant	T/C	snv	4.0E-06		100
rs17782313		0.683	0.480	18	60183864	intergenic variant	T/C	snv		0.24	34
rs1800247	BGLAP ; PMF1-BGLAP	0.882	0.200	1	156242034	intron variant	T/C	snv		0.20	4
rs1805081	NPC1	0.925	0.120	18	23560468	missense variant	T/C	snv	0.33	0.29	3
rs225014	DIO2	0.695	0.400	14	80203237	missense variant	T/C	snv	0.41	0.39	22
rs2273773	SIRT1	0.790	0.360	10	67906841	synonymous variant	T/C	snv	0.11	7.1E-02	9
rs2281939	SORBS1	0.790	0.320	10	95414595	missense variant	T/C	snv	8.2E-02	0.13	9
rs25487	XRCC1	0.441	0.800	19	43551574	missense variant	T/C	snv	0.68	0.71	205
rs2943641		0.763	0.160	2	226229029	intergenic variant	T/C	snv		0.67	18
rs35518301	HBD	0.827	0.200	11	5234514	5 prime UTR variant	T/C	snv			6
rs3782886	BRAP	0.724	0.480	12	111672685	synonymous variant	T/C	snv	1.9E-02	5.9E-03	22
rs429358	APOE	0.590	0.600	19	44908684	missense variant	T/C	snv	0.14	0.16	66
rs562962093	MBL2	0.742	0.520	10	52771740	upstream gene variant	T/C	snv		7.0E-06	13
rs662	PON1	0.485	0.840	7	95308134	missense variant	T/C	snv	0.38	0.42	157