DisGeNET - a database of gene-disease associations

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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
rs1167998	DOCK7			1	62465961	intron variant	C/A	snv		0.57	5
rs1748197	DOCK7			1	62590441	intron variant	G/A	snv		0.42	5
rs2131925	DOCK7			1	62560271	intron variant	G/T	snv		0.57	5
rs10789117	DOCK7 ; ANGPTL3			1	62606594	intron variant	A/C;T	snv			5
rs11207997	DOCK7 ; ANGPTL3			1	62596235	intron variant	C/T	snv		0.39	5
rs10889353	DOCK7			1	62652525	intron variant	A/C;T	snv			3
rs1748195	DOCK7	0.851	0.120	1	62583922	intron variant	C/G;T	snv			3
rs10889338	DOCK7			1	62519226	intron variant	C/T	snv		0.34	2
rs11207995	DOCK7			1	62583880	intron variant	A/C;G	snv			2
rs1168013	DOCK7	1.000	0.120	1	62531167	intron variant	C/G;T	snv			2
rs1168045	DOCK7			1	62517220	intron variant	C/A;T	snv			2
rs1168046	DOCK7			1	62518022	intron variant	A/C;G	snv			2
rs1168047	DOCK7			1	62518080	intron variant	C/A;T	snv			2
rs1168050	DOCK7			1	62521284	intron variant	C/A;T	snv		0.58	2
rs1168097	DOCK7			1	62654700	intron variant	C/T	snv		0.57	2
rs12042319	DOCK7	1.000	0.040	1	62584148	3 prime UTR variant	G/A	snv		0.36	2
rs12048208	DOCK7			1	62589609	intron variant	G/A	snv		0.12	2
rs12090886	DOCK7			1	62515769	intron variant	G/A	snv		0.57	2
rs636523	DOCK7			1	62454337	non coding transcript exon variant	A/G	snv		0.36	2
rs10889333	DOCK7			1	62491359	intron variant	G/A	snv		0.33	1
rs10889348	DOCK7			1	62612551	intron variant	A/T	snv		0.32	1
rs11208004	DOCK7			1	62679768	intron variant	G/A	snv		0.33	1
rs12047226	DOCK7			1	62639867	intron variant	T/A;C	snv			1
rs12239736	DOCK7			1	62620326	intron variant	T/A	snv		0.38	1
rs3850634	DOCK7			1	62584927	intron variant	T/G	snv	0.33	0.34	1