DisGeNET - a database of gene-disease associations

Source: UNIPROT

Variants associated to the Disease: Stage IV Skin Melanoma ×

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
rs121913254	NRAS	0.658	0.440	1	114713909	stop gained	G/A;C;T	snv			2
rs267604273	ADAM10	1.000	0.080	15	58665156	missense variant	G/A	snv			1
rs151030407	ADAM12	1.000	0.080	10	126017332	missense variant	G/A;C	snv	5.0E-05	4.9E-05	1
rs267601916	ADAM18	1.000	0.080	8	39610692	missense variant	C/T	snv			1
rs267601918	ADAM18	1.000	0.080	8	39645460	missense variant	G/A	snv			1
rs267601860	ADAM28 ; LOC101929294	1.000	0.080	8	24313405	missense variant	G/A	snv	4.0E-06		1
rs267601864	ADAM28 ; LOC101929294	1.000	0.080	8	24335579	missense variant	G/A	snv			1
rs140083180	ADAM29	1.000	0.080	4	174976294	missense variant	A/T	snv			1
rs150047888	ADAM29	1.000	0.080	4	174976733	missense variant	G/A	snv	8.0E-06		1
rs267600087	ADAM29	1.000	0.080	4	174975856	missense variant	G/A	snv			1
rs267600089	ADAM29	1.000	0.080	4	174976439	missense variant	G/A	snv	4.2E-06		1
rs267600090	ADAM29	1.000	0.080	4	174976558	missense variant	G/A	snv			1
rs267600091	ADAM29	1.000	0.080	4	174976826	missense variant	G/A	snv			1
rs267600093	ADAM29	1.000	0.080	4	174977122	missense variant	C/T	snv			1
rs866380131	ADAM29	1.000	0.080	4	174976226	missense variant	C/T	snv			1
rs899870236	ADAM29	1.000	0.080	4	174976051	missense variant	G/A	snv			1
rs1169229302	ADAM33	1.000	0.080	20	3673650	missense variant	G/A	snv			1
rs267601867	ADAM7 ; LOC101929294	1.000	0.080	8	24465702	missense variant	C/G;T	snv	1.2E-05		1
rs113488022	BRAF	0.351	0.840	7	140753336	missense variant	A/C;G;T	snv	4.0E-06		1
rs267601862	LOC101929294 ; ADAM28	1.000	0.080	8	24332727	missense variant	G/A	snv			1
rs137990671	LOC101929294 ; ADAM7	1.000	0.080	8	24442511	missense variant	C/A;T	snv			1
rs150319320	LOC101929294 ; ADAM7	1.000	0.080	8	24441148	missense variant	C/T	snv			1
rs267601866	LOC101929294 ; ADAM7	1.000	0.080	8	24442526	missense variant	C/T	snv			1
rs267601868	LOC101929294 ; ADAM7	1.000	0.080	8	24487303	missense variant	G/A	snv			1
rs1034941983	LOC101929294 ; ADAM7 ; LOC101929315	1.000	0.080	8	24499308	missense variant	G/A	snv			1