DisGeNET - a database of gene-disease associations

List of shared variants

Malignant Uterine Corpus Neoplasm, C0153574

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 EXOME	Num. diseases
rs28934576	TP53	0.554	0.600	17	7673802	missense variant	C/A;G;T	snv	4.0E-06; 1.6E-05	78
rs11554290	NRAS	0.583	0.600	1	114713908	missense variant	T/A;C;G	snv		59
rs11540652	TP53	0.592	0.640	17	7674220	missense variant	C/A;G;T	snv	1.2E-05	57
rs121912651	TP53	0.605	0.680	17	7674221	missense variant	G/A;C	snv	4.0E-06	53
rs121913237	NRAS	0.611	0.560	1	114716126	missense variant	C/A;G;T	snv	8.0E-06	50
rs104894228	LRRC56 ; HRAS	0.605	0.560	11	534286	missense variant	C/A;G;T	snv		48
rs121913343	TP53	0.611	0.520	17	7673803	missense variant	G/A;C;T	snv	1.2E-05	44
rs121913233	HRAS ; LRRC56	0.627	0.520	11	533874	missense variant	T/A;C;G	snv		37
rs121913364	BRAF	0.641	0.520	7	140753334	missense variant	T/C;G	snv	4.0E-06	34
rs104894226	LRRC56 ; HRAS	0.658	0.560	11	534285	missense variant	C/A;G;T	snv		29
rs17851045	KRAS	0.672	0.400	12	25227341	missense variant	T/A;G	snv	4.0E-06	27
rs28933406	LRRC56 ; HRAS	0.667	0.480	11	533875	missense variant	G/C;T	snv		27
rs121913255	NRAS	0.667	0.400	1	114713907	missense variant	T/A;G	snv		26
rs121913250	NRAS	0.683	0.440	1	114716127	missense variant	C/A;G;T	snv		25
rs138729528	TP53	0.677	0.480	17	7675089	missense variant	G/A;C	snv	1.6E-05	25
rs764146326	TP53	0.662	0.480	17	7673779	missense variant	C/A;G;T	snv	4.0E-06	25
rs786201838	TP53	0.683	0.440	17	7674953	missense variant	T/A;C;G	snv		24
rs876658468	TP53	0.689	0.440	17	7674954	missense variant	G/A;C;T	snv		24
rs1057519981	TP53	0.689	0.440	17	7674251	missense variant	A/C;G;T	snv		22
rs193920774	TP53	0.695	0.440	17	7673823	missense variant	C/A;T	snv		22
rs587781525	TP53	0.689	0.480	17	7673778	missense variant	T/A;C;G	snv		22
rs876660821	TP53	0.689	0.400	17	7675075	missense variant	A/C;G;T	snv		22
rs730882005	TP53	0.701	0.400	17	7674250	missense variant	C/A;G;T	snv	8.0E-06	20
rs1057519895	FBXW7	0.724	0.240	4	152328232	missense variant	C/A;G;T	snv		17
rs149680468	FBXW7	0.742	0.320	4	152326137	missense variant	G/A;C;T	snv		15