DisGeNET - a database of gene-disease associations

List of shared variants

Squamous cell carcinoma of the head and neck, C1168401

Disease: Adenocarcinoma of prostate

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
rs1057519909	MAP2K1	0.790	0.240	15	66435116	missense variant	A/C	snv		6
rs1057519939	PIK3CA	0.776	0.160	3	179203763	missense variant	A/C	snv		10
rs1057519927	PIK3CA	0.716	0.240	3	179218295	missense variant	A/C;G;T	snv		18
rs1057519978	TP53	0.763	0.360	17	7675191	missense variant	A/C;G;T	snv		12
rs121913274	PIK3CA	0.645	0.320	3	179218304	missense variant	A/C;G;T	snv		28
rs397517201	PIK3CA	0.732	0.240	3	179218307	missense variant	A/C;G;T	snv		14
rs530941076	TP53	0.695	0.280	17	7674873	missense variant	A/C;G;T	snv	4.0E-06	20
rs587782289	TP53	0.752	0.240	17	7674257	missense variant	A/C;G;T	snv		12
rs864622237	TP53	0.716	0.320	17	7674263	missense variant	A/C;G;T	snv		17
rs967461896	TP53	0.724	0.240	17	7675086	missense variant	A/C;G;T	snv		16
rs1057519938	PIK3CA	0.776	0.160	3	179203764	missense variant	A/C;T	snv		10
rs121913279	PIK3CA	0.526	0.560	3	179234297	missense variant	A/G;T	snv	4.0E-06; 4.0E-06	45
rs121913286	PIK3CA	0.677	0.280	3	179218306	missense variant	C/A;G	snv		20
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
rs121912656	TP53	0.662	0.560	17	7674229	missense variant	C/A;G;T	snv	4.0E-06; 4.0E-06	20
rs121913496	LRRC56 ; HRAS	0.724	0.440	11	533873	missense variant	C/A;G;T	snv		11
rs28934575	TP53	0.641	0.400	17	7674230	missense variant	C/A;G;T	snv		25
rs28934576	TP53	0.554	0.600	17	7673802	missense variant	C/A;G;T	snv	4.0E-06; 1.6E-05	39
rs587778720	TP53	0.667	0.360	17	7674893	missense variant	C/A;G;T	snv	4.0E-06	25
rs587782329	TP53	0.677	0.280	17	7674217	missense variant	C/A;G;T	snv		16
rs730882008	TP53	0.683	0.440	17	7673775	missense variant	C/A;G;T	snv	4.0E-06	22
rs587781288	TP53	0.732	0.440	17	7675190	missense variant	C/A;T	snv		15
rs786202962	TP53	0.701	0.320	17	7675085	missense variant	C/A;T	snv	4.0E-06	17