DisGeNET - a database of gene-disease associations

List of shared variants

Leukemia, Myelocytic, Acute, C0023467

Disease: Neoplastic Syndromes, Hereditary

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	AF GENOME	Num. diseases
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
rs121913343	TP53	0.611	0.520	17	7673803	missense variant	G/A;C;T	snv	1.2E-05		29
rs121912666	TP53	0.645	0.360	17	7674872	missense variant	T/C;G	snv	8.0E-06		24
rs786201057	TP53	0.677	0.400	17	7675995	missense variant	G/A;C;T	snv			24
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
rs753660142	TP53	0.708	0.280	17	7673782	missense variant	T/C;G	snv	1.6E-05		19
rs786201059	TP53	0.701	0.360	17	7673764	stop gained	C/A;G;T	snv			19
rs121912660	TP53	0.683	0.240	17	7673781	missense variant	C/A;G;T	snv			18
rs1057519747	TP53	0.716	0.280	17	7675094	missense variant	A/C;G;T	snv			17
rs786202962	TP53	0.701	0.320	17	7675085	missense variant	C/A;T	snv	4.0E-06		17
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
rs587782177	TP53	0.763	0.200	17	7674887	missense variant	C/A;G;T	snv			11