DisGeNET - a database of gene-disease associations

List of shared variants

Leukemia, Myelocytic, Acute, C0023467

Disease: Malignant Uterine Corpus Neoplasm

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
rs104894229	LRRC56 ; HRAS	0.564	0.600	11	534289	missense variant	C/A;G;T	snv		52
rs11540652	TP53	0.592	0.640	17	7674220	missense variant	C/A;G;T	snv	1.2E-05	42
rs28934576	TP53	0.554	0.600	17	7673802	missense variant	C/A;G;T	snv	4.0E-06; 1.6E-05	39
rs121912651	TP53	0.605	0.680	17	7674221	missense variant	G/A;C	snv	4.0E-06	37
rs104894230	HRAS ; LRRC56	0.564	0.600	11	534288	missense variant	C/A;G;T	snv		36
rs104894228	LRRC56 ; HRAS	0.605	0.560	11	534286	missense variant	C/A;G;T	snv		30
rs121913343	TP53	0.611	0.520	17	7673803	missense variant	G/A;C;T	snv	1.2E-05	29
rs11554290	NRAS	0.583	0.600	1	114713908	missense variant	T/A;C;G	snv		25
rs121912666	TP53	0.645	0.360	17	7674872	missense variant	T/C;G	snv	8.0E-06	24
rs104894226	LRRC56 ; HRAS	0.658	0.560	11	534285	missense variant	C/A;G;T	snv		23
rs587780070	TP53	0.683	0.320	17	7675077	missense variant	G/A;C;T	snv	4.0E-06	23
rs786201838	TP53	0.683	0.440	17	7674953	missense variant	T/A;C;G	snv		23
rs876658468	TP53	0.689	0.440	17	7674954	missense variant	G/A;C;T	snv		22
rs876660821	TP53	0.689	0.400	17	7675075	missense variant	A/C;G;T	snv		21
rs121913233	HRAS ; LRRC56	0.627	0.520	11	533874	missense variant	T/A;C;G	snv		20
rs1057519991	TP53	0.662	0.440	17	7675076	missense variant	T/A;C;G	snv	4.0E-06	19
rs121913255	NRAS	0.667	0.400	1	114713907	missense variant	T/A;G	snv		19
rs1057519747	TP53	0.716	0.280	17	7675094	missense variant	A/C;G;T	snv		17
rs28933406	LRRC56 ; HRAS	0.667	0.480	11	533875	missense variant	G/C;T	snv		17
rs587782329	TP53	0.677	0.280	17	7674217	missense variant	C/A;G;T	snv		16
rs17851045	KRAS	0.672	0.400	12	25227341	missense variant	T/A;G	snv	4.0E-06	15
rs587781288	TP53	0.732	0.440	17	7675190	missense variant	C/A;T	snv		15
rs1057519977	TP53	0.763	0.360	17	7675189	missense variant	G/C	snv		13
rs1057519978	TP53	0.763	0.360	17	7675191	missense variant	A/C;G;T	snv		12
rs121913237	NRAS	0.611	0.560	1	114716126	missense variant	C/A;G;T	snv	8.0E-06	12