DisGeNET - a database of gene-disease associations

List of shared variants

Glioblastoma, C0017636

Disease: Uterine Cervical Neoplasm

Source: INFERRED ×

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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
rs121913279	PIK3CA	0.526	0.560	3	179234297	missense variant	A/G;T	snv	4.0E-06; 4.0E-06	45
rs121913281	PIK3CA	0.623	0.520	3	179234296	missense variant	C/T	snv		37
rs104894230	HRAS ; LRRC56	0.564	0.600	11	534288	missense variant	C/A;G;T	snv		36
rs121909224	PTEN	0.627	0.560	10	87933147	stop gained	C/G;T	snv	1.2E-05	35
rs104886003	PIK3CA	0.562	0.440	3	179218303	missense variant	G/A;C	snv	4.0E-06	34
rs121913274	PIK3CA	0.645	0.320	3	179218304	missense variant	A/C;G;T	snv		28
rs121913275	PIK3CA	0.672	0.320	3	179218305	missense variant	G/A;C;T	snv	4.0E-06	25
rs121909229	PTEN	0.683	0.400	10	87933148	missense variant	G/A;C;T	snv		23
rs1057519932	PIK3CA	0.683	0.320	3	179234298	missense variant	T/G	snv		22
rs121913273	PIK3CA	0.605	0.440	3	179218294	missense variant	G/A;C	snv		21
rs1057519981	TP53	0.689	0.440	17	7674251	missense variant	A/C;G;T	snv		20
rs121913286	PIK3CA	0.677	0.280	3	179218306	missense variant	C/A;G	snv		20
rs730882005	TP53	0.701	0.400	17	7674250	missense variant	C/A;G;T	snv	8.0E-06	20
rs1057519927	PIK3CA	0.716	0.240	3	179218295	missense variant	A/C;G;T	snv		18
rs747342068	TP53	0.695	0.440	17	7675218	missense variant	T/C;G	snv	4.0E-06	17
rs866775781	TP53	0.716	0.440	17	7675216	splice acceptor variant	C/A;G	snv		17
rs1057519996	TP53	0.701	0.360	17	7675217	splice acceptor variant	T/A;C;G	snv		16
rs1057519942	PIK3CA	0.724	0.320	3	179203760	missense variant	G/A	snv		15
rs397517201	PIK3CA	0.732	0.240	3	179218307	missense variant	A/C;G;T	snv		14
rs1057519940	PIK3CA	0.752	0.200	3	179218308	missense variant	G/T	snv		13
rs398124146	CREBBP	0.742	0.360	16	3738617	missense variant	G/A;C	snv		12
rs587777790	PIK3CA	0.732	0.280	3	179199690	missense variant	G/A	snv		12
rs747241612	FBXW7	0.752	0.240	4	152326215	missense variant	G/C	snv	4.0E-06	12
rs866987936	FBXW7	0.752	0.240	4	152326214	missense variant	C/A;G;T	snv		12