DisGeNET - a database of gene-disease associations

List of shared variants

Cutaneous Melanoma, C0151779

Disease: Multiple Myeloma

Source: CLINVAR ×

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	Num. diseases
rs1023835002	B2M ; PATL2	0.763	0.280	15	44711547	start lost	A/G;T	snv		10
rs104894226	LRRC56 ; HRAS	0.658	0.560	11	534285	missense variant	C/A;G;T	snv		23
rs104894228	LRRC56 ; HRAS	0.605	0.560	11	534286	missense variant	C/A;G;T	snv		30
rs104894229	LRRC56 ; HRAS	0.564	0.600	11	534289	missense variant	C/A;G;T	snv		52
rs104894230	HRAS ; LRRC56	0.564	0.600	11	534288	missense variant	C/A;G;T	snv		36
rs104894340	CDK4	0.827	0.200	12	57751647	missense variant	C/A;T	snv		5
rs1057519877	B2M ; PATL2	0.763	0.280	15	44711549	start lost	G/A	snv		10
rs1057519879	PATL2 ; B2M	0.763	0.280	15	44711548	start lost	T/C;G	snv		10
rs1057519983	TP53	0.724	0.360	17	7673797	missense variant	A/G	snv		16
rs113488022	BRAF	0.351	0.840	7	140753336	missense variant	A/C;G;T	snv	4.0E-06	22
rs11540652	TP53	0.592	0.640	17	7674220	missense variant	C/A;G;T	snv	1.2E-05	42
rs11547328	CDK4	0.701	0.360	12	57751648	missense variant	G/A;T	snv	4.0E-06	6
rs11554290	NRAS	0.583	0.600	1	114713908	missense variant	T/A;C;G	snv		25
rs121434595	NRAS	0.708	0.320	1	114716124	missense variant	C/A;G;T	snv		13
rs121434596	NRAS	0.677	0.440	1	114716123	missense variant	C/A;G;T	snv	4.0E-06; 4.0E-06	14
rs121912651	TP53	0.605	0.680	17	7674221	missense variant	G/A;C	snv	4.0E-06	37
rs121913233	HRAS ; LRRC56	0.627	0.520	11	533874	missense variant	T/A;C;G	snv		20
rs121913237	NRAS	0.611	0.560	1	114716126	missense variant	C/A;G;T	snv	8.0E-06	12
rs121913250	NRAS	0.683	0.440	1	114716127	missense variant	C/A;G;T	snv		12
rs121913255	NRAS	0.667	0.400	1	114713907	missense variant	T/A;G	snv		19
rs121913338	BRAF	0.677	0.400	7	140753354	missense variant	T/A;C;G	snv		12
rs121913343	TP53	0.611	0.520	17	7673803	missense variant	G/A;C;T	snv	1.2E-05	29
rs121913351	BRAF	0.776	0.240	7	140781611	missense variant	C/A;G;T	snv	4.0E-06	9
rs121913355	BRAF	0.641	0.520	7	140781602	missense variant	C/A;G;T	snv	4.0E-06	32
rs121913357	BRAF	0.742	0.320	7	140781603	stop gained	C/A;G;T	snv		11