DisGeNET - a database of gene-disease associations

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
rs1362739	EXOC4	1.000	0.040	7	133746181	intron variant	C/A;T	snv	0.48	2
rs6949760	EXOC4			7	133991348	intron variant	C/A	snv	0.73	2
rs10215367	EXOC4			7	133260999	intron variant	C/T	snv	0.68	1
rs10254118	EXOC4			7	133473599	intron variant	T/A	snv	0.29	1
rs10281827	EXOC4			7	133397056	intron variant	A/G;T	snv		1
rs1030268	EXOC4			7	133921878	intron variant	A/G;T	snv		1
rs10954428	EXOC4			7	133703303	intron variant	G/A	snv	0.34	1
rs11765450	EXOC4			7	133384928	intron variant	C/T	snv	0.14	1
rs11977339	EXOC4			7	133285920	intron variant	C/T	snv	0.30	1
rs12707087	EXOC4			7	133269778	intron variant	T/C	snv	0.86	1
rs12707093	EXOC4			7	133516063	intron variant	C/G;T	snv		1
rs12707116	EXOC4			7	133740156	intron variant	T/C	snv	0.48	1
rs17167170	EXOC4			7	133617591	intron variant	A/G	snv	0.21	1
rs17167210	EXOC4			7	133654590	intron variant	G/A	snv	0.41	1
rs1882538	EXOC4			7	133276984	intron variant	G/A;T	snv		1
rs2346268	EXOC4			7	133957989	intron variant	G/A	snv	0.69	1
rs2346449	EXOC4			7	134049164	intron variant	G/T	snv	0.73	1
rs2971963	EXOC4			7	133956752	intron variant	A/G;T	snv		1
rs2971970	EXOC4			7	133959025	intron variant	T/G	snv	0.85	1
rs35284403	EXOC4			7	133264129	intron variant	T/C	snv	0.30	1
rs3823572	EXOC4			7	133995848	intron variant	G/A	snv	0.52	1
rs4422723	EXOC4			7	133921405	intron variant	A/T	snv	0.62	1
rs4728302	EXOC4			7	133945710	intron variant	C/T	snv	0.53	1
rs4731992	EXOC4			7	134017344	intron variant	A/G	snv	0.85	1
rs6949831	EXOC4			7	133396716	intron variant	G/A;C	snv		1