DisGeNET - a database of gene-disease associations

Source: GWASCAT ×

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
rs964184	ZPR1	0.716	0.440	11	116778201	3 prime UTR variant	G/C	snv		0.82	35
rs4420638	APOC1	0.708	0.520	19	44919689	downstream gene variant	A/G	snv		0.18	30
rs429358	APOE	0.590	0.600	19	44908684	missense variant	T/C	snv	0.14	0.16	26
rs7412	APOE	0.641	0.640	19	44908822	missense variant	C/T	snv	6.2E-02	7.9E-02	20
rs5744680	POLK	0.851	0.120	5	75584065	intron variant	G/A	snv		0.55	18
rs2954021		1.000	0.040	8	125469835	intron variant	A/G	snv		0.54	13
rs1558902	FTO	0.827	0.120	16	53769662	intron variant	T/A	snv		0.31	12
rs115849089				8	20054859	intergenic variant	G/A	snv		9.8E-02	7
rs116843064	ANGPTL4	0.776	0.160	19	8364439	missense variant	G/A	snv	1.3E-02	1.5E-02	7
rs863750	ZNF664-RFLNA ; RFLNA			12	124020897	intron variant	C/T	snv		0.53	7
rs1042034	APOB	0.851	0.240	2	21002409	missense variant	C/T	snv	0.70	0.78	6
rs112259268				17	43797377	downstream gene variant	C/A	snv		1.9E-02	6
rs1126930	PRKAG1 ; DDN-AS1			12	49005349	missense variant	G/C	snv	2.1E-02	2.1E-02	5
rs3768321	PABPC4 ; PABPC4-AS1	1.000	0.080	1	39570256	intron variant	G/T	snv		0.14	5
rs72959041	RSPO3			6	127133748	intron variant	G/A	snv		3.2E-02	5
rs77960347	LIPG			18	49583585	missense variant	A/C;G	snv	4.0E-06; 8.7E-03		5
rs55747707	MLXIPL			7	73623036	intron variant	G/A	snv		0.16	4
rs7679	PCIF1	0.925	0.160	20	45947863	3 prime UTR variant	T/C	snv		0.13	4
rs12145743	RRNAD1			1	156730859	intron variant	T/G	snv		0.24	3
rs380267				19	54295230	upstream gene variant	G/A	snv		0.82	3
rs7726839	CEP72			5	618471	intron variant	A/G	snv		0.31	3