DisGeNET - a database of gene-disease associations

List of shared variants

Carcinogenesis, C0596263

Disease: Neoplasms

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	AF GENOME	Num. diseases
rs1457127715	ERBB2			17	39715810	missense variant	G/A;C	snv	4.0E-06		2
rs573154688	TP53	1.000	0.160	17	7670711	missense variant	C/T	snv	4.4E-05	3.5E-05	3
rs80291436	VCX	1.000	0.080	X	7843706	missense variant	T/A;C;G	snv	4.9E-05; 0.19		3
rs1267580705	EPAS1	0.925	0.240	2	46360680	missense variant	G/A	snv			4
rs12774070	ADAMTS14	0.925	0.120	10	70753879	missense variant	C/A;G	snv	0.23	0.19	4
rs1452231640	POLB	1.000	0.080	8	42339015	missense variant	T/C	snv	4.0E-06		4
rs765189442	ABCB11	0.925	0.080	2	168995422	missense variant	T/C	snv	8.1E-06		4
rs1188536960	SORD	0.882	0.120	15	45043305	missense variant	A/G	snv			5
rs121908586	PDGFRA	1.000	0.080	4	54274869	missense variant	T/A;C	snv			5
rs28933369	MIR4728 ; ERBB2	0.925	0.080	17	39724744	missense variant	G/A	snv			5
rs779196500	TP53	0.882	0.120	17	7675187	missense variant	G/A	snv	4.0E-06		5
rs1057519853	GNAQ	0.851	0.080	9	77794572	missense variant	TG/AA	mnv			6
rs1332018	GSTM5 ; GSTM3	0.882	0.200	1	109740350	5 prime UTR variant	G/T	snv	0.64	0.66	6
rs17878467	BIRC5	0.925	0.080	17	78214076	upstream gene variant	C/G;T	snv			6
rs188957694	ESR1	0.882	0.080	6	151944218	missense variant	G/A;C	snv	4.0E-05	4.9E-05	6
rs61573157	ADAMTS14	0.882	0.160	10	70760503	missense variant	C/T	snv	8.6E-02	7.5E-02	6
rs798766	TACC3	0.851	0.120	4	1732512	intron variant	T/C	snv		0.76	6
rs121912665	TP53	1.000	0.120	17	7674965	missense variant	G/A	snv	2.4E-05	7.0E-06	7
rs17822931	ABCC11	0.827	0.080	16	48224287	missense variant	C/G;T	snv	4.0E-06; 0.22	0.13	7
rs267601395	EZH2	0.925	0.160	7	148811636	missense variant	A/G;T	snv			7
rs34589476	MET	0.827	0.160	7	116771869	missense variant	C/T	snv	2.9E-03	3.2E-03	7
rs41291957	CARMN ; MIR145 ; MIR143	0.882	0.200	5	149428827	intron variant	G/A	snv		0.12	7
rs762292600	ESR1	0.925	0.080	6	151944316	missense variant	A/G	snv	4.0E-06	1.4E-05	7
rs763193414	ERBB2	0.827	0.160	17	39707034	missense variant	G/A	snv	3.7E-05	4.9E-05	7
rs7664413	VEGFC ; LOC105377555	0.851	0.160	4	176687553	intron variant	C/T	snv	0.24	0.25	7