DisGeNET - a database of gene-disease associations

List of shared variants

Cutaneous Melanoma, C0151779

Disease: Multiple Myeloma

Source: CLINVAR ×

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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	Num. diseases
rs113488022	BRAF	0.351	0.840	7	140753336	missense variant	A/C;G;T	snv	4.0E-06	22
rs121913366	BRAF	0.763	0.400	7	140753345	missense variant	A/C;T	snv		6
rs1057519983	TP53	0.724	0.360	17	7673797	missense variant	A/G	snv		16
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
rs11540652	TP53	0.592	0.640	17	7674220	missense variant	C/A;G;T	snv	1.2E-05	42
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
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
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
rs121913500	IDH1	0.529	0.600	2	208248388	missense variant	C/A;G;T	snv	4.0E-06	18
rs28934576	TP53	0.554	0.600	17	7673802	missense variant	C/A;G;T	snv	4.0E-06; 1.6E-05	39
rs483352697	TP53	0.695	0.480	17	7674944	missense variant	C/A;G;T	snv	4.0E-06	17
rs764146326	TP53	0.662	0.480	17	7673779	missense variant	C/A;G;T	snv	4.0E-06	20
rs863224451	TP53	0.701	0.440	17	7673796	missense variant	C/A;G;T	snv		19
rs104894340	CDK4	0.827	0.200	12	57751647	missense variant	C/A;T	snv		5
rs397516896	BRAF	0.763	0.360	7	140753355	missense variant	C/G;T	snv		11
rs1057519877	B2M ; PATL2	0.763	0.280	15	44711549	start lost	G/A	snv		10
rs121912651	TP53	0.605	0.680	17	7674221	missense variant	G/A;C	snv	4.0E-06	37