DisGeNET - a database of gene-disease associations

List of shared variants

Multiple Myeloma, C0026764

Disease: Chronic Lymphocytic Leukemia

Source: ALL

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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 GENOME	Num. diseases
rs104894226	LRRC56 ; HRAS	0.658	0.560	11	534285	missense variant	C/A;G;T	snv		29
rs104894228	LRRC56 ; HRAS	0.605	0.560	11	534286	missense variant	C/A;G;T	snv		48
rs1050976	IRF4	0.851	0.280	6	408079	3 prime UTR variant	C/T	snv	0.37	4
rs1057519981	TP53	0.689	0.440	17	7674251	missense variant	A/C;G;T	snv		22
rs1057519983	TP53	0.724	0.360	17	7673797	missense variant	A/G	snv		16
rs1131691014	TP53	0.439	0.800	17	7676154	frameshift variant	-/C	ins		214
rs11554290	NRAS	0.583	0.600	1	114713908	missense variant	T/A;C;G	snv		59
rs11715604	NCK1	0.851	0.160	3	136870707	intron variant	A/G;T	snv		4
rs121913233	HRAS ; LRRC56	0.627	0.520	11	533874	missense variant	T/A;C;G	snv		37
rs121913240	KRAS	0.672	0.440	12	25227342	missense variant	T/A;C;G	snv		24
rs121913250	NRAS	0.683	0.440	1	114716127	missense variant	C/A;G;T	snv		25
rs121913255	NRAS	0.667	0.400	1	114713907	missense variant	T/A;G	snv		26
rs121913338	BRAF	0.677	0.400	7	140753354	missense variant	T/A;C;G	snv		24
rs121913377	BRAF	0.354	0.840	7	140753335	missense variant	CA/AT;TT	mnv		480
rs12638862		0.827	0.160	3	169759718	downstream gene variant	A/G	snv	0.24	10
rs12711846	MIR4435-2HG ; ACOXL-AS1 ; ACOXL	0.851	0.160	2	111098716	non coding transcript exon variant	A/G	snv	0.26	4
rs13069553		0.851	0.200	3	169790484	upstream gene variant	A/G	snv	0.21	4
rs131821	NCAPH2	0.851	0.160	22	50511648	intron variant	T/-;TT;TTT;TTTT	delins		4
rs149207840	SP140	0.851	0.160	2	230279864	intron variant	CTGCCTC/-;CTGCCTCCTGCCTC	delins	0.15	4
rs181181503	LOC100507377	0.851	0.160	12	74276187	intron variant	T/C	snv	1.5E-03	4
rs2010963	VEGFA	0.542	0.840	6	43770613	5 prime UTR variant	C/G	snv	0.68	82
rs210143	GGNBP1 ; BAK1	0.827	0.160	6	33579153	intron variant	T/C	snv	0.74	6
rs2456449	CASC19 ; PCAT1	0.827	0.280	8	127180736	intron variant	A/G	snv	0.30	5
rs2546191	ELL2	0.851	0.160	5	95896837	intron variant	G/A	snv	0.38	4
rs2720680	PVT1	0.851	0.160	8	128102971	intron variant	A/G	snv	0.33	4