DisGeNET - a database of gene-disease associations

Source: GWASDB ×

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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 GENOME	Num. diseases
rs4362077	ABCC2			10	99828664	intron variant	C/T	snv	1.6E-02	2
rs7811025				7	99788078	upstream gene variant	C/T	snv	4.8E-02	4
rs11568767	TGFBR1			9	99132990	intron variant	C/T	snv	3.7E-03	4
rs11568746	TGFBR1			9	99105926	intron variant	C/G	snv	2.1E-05	6
rs2602836	LOC100507053			4	99093654	intron variant	A/G	snv	0.50	2
rs10818782	GABBR2			9	98325004	intron variant	G/A	snv	0.60	2
rs9556465	ABCC4			13	95205263	intron variant	G/T	snv	3.4E-03	2
rs11938688	HPGDS			4	94336456	intron variant	C/G	snv	4.0E-02	2
rs11941250	HPGDS			4	94308312	intron variant	G/A;C	snv		2
rs1461729	LOC157273	1.000		8	9329732	intron variant	A/G	snv	0.88	3
rs2126259	LOC157273	1.000		8	9327636	intron variant	T/C	snv	0.87	7
rs9987289	LOC157273	1.000	0.040	8	9325848	non coding transcript exon variant	A/G	snv	0.87	8
rs6694527	SLC2A5			1	9058969	intron variant	G/A	snv	2.4E-02	2
rs16942333	ACAN			15	88845033	intron variant	A/G	snv	3.3E-02	3
rs3822072	FAM13A			4	88820118	intron variant	G/A;C	snv		4
rs16880248	CNR1			6	88141968	3 prime UTR variant	G/T	snv	2.7E-02	5
rs12242772	PTEN			10	87944637	intron variant	A/G	snv	3.0E-02	3
rs2967605	RAB11B	0.925	0.040	19	8404854	downstream gene variant	C/T	snv	0.20	3
rs7255436	ANGPTL4			19	8368312	intron variant	C/A	snv	0.55	2
rs2278236	ANGPTL4			19	8366697	intron variant	G/A;C	snv		2
rs7081526	NRG3			10	82162648	intron variant	G/A	snv	7.1E-02	2
rs7895300	NRG3			10	82091203	intron variant	C/A;G;T	snv		2
rs5745642	HGF			7	81756276	3 prime UTR variant	G/C	snv	1.6E-02	2
rs2925979	CMIP	1.000	0.080	16	81501185	intron variant	T/A;C	snv		3
rs2366858				7	80711306	regulatory region variant	C/A	snv	0.94	2