DisGeNET - a database of gene-disease associations

Source: GWASDB ×

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 GENOME	Num. diseases
rs9998785	EXOSC9			4	121807810	non coding transcript exon variant	A/T	snv	0.29	1
rs9995319	BBS7			4	121849522	intron variant	G/C	snv	0.29	1
rs9990333				3	196100334	intergenic variant	C/T	snv	0.42	1
rs9972882	STARD3	0.925	0.080	17	39651445	intron variant	A/C	snv	0.66	1
rs9967849	MIR4432HG			2	60382339	intron variant	C/T	snv	0.33	3
rs9963843	C18orf25			18	46262655	intron variant	C/A;T	snv		1
rs9963153	C18orf25			18	46260101	intron variant	T/C	snv	0.72	1
rs9959905	C18orf25			18	46231084	intron variant	A/G;T	snv		1
rs9959813	C18orf25			18	46261119	intron variant	A/G	snv	0.74	1
rs99595				20	57414752	regulatory region variant	C/G;T	snv		1
rs995716				4	54500464	intergenic variant	G/C	snv	0.37	1
rs9956574	C18orf25			18	46202237	intron variant	C/T	snv	0.72	1
rs9955853	C18orf25			18	46249689	intron variant	C/T	snv	0.43	1
rs9955008				18	46078922	upstream gene variant	G/A	snv	0.59	1
rs9952469	C18orf25			18	46232044	3 prime UTR variant	T/C	snv	0.65	1
rs9950234	PSTPIP2			18	46073234	upstream gene variant	T/C	snv	0.59	1
rs9949494	C18orf25			18	46231334	intron variant	T/C	snv	0.61	1
rs9947316	C18orf25			18	46197865	intron variant	T/A;G	snv		1
rs9945783	C18orf25			18	46202294	intron variant	T/C	snv	0.61	1
rs9944836	C18orf25			18	46251414	intron variant	A/G;T	snv		1
rs9944767	C18orf25			18	46251091	intron variant	G/A	snv	0.74	1
rs9944411	FBXL20			17	39327346	intron variant	T/C	snv	0.32	2
rs994379				6	26305179	intergenic variant	G/C	snv	0.54	1
rs9938020	NFATC3			16	68217881	3 prime UTR variant	C/G	snv	0.21	1
rs9933309	PIEZO1			16	88778524	intron variant	T/C	snv	0.72	1