DisGeNET - a database of gene-disease associations

List of shared variants

Neoplasms, C0027651

Disease: Non-Small Cell Lung Carcinoma

Source: ALL

Results per page

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
rs1048977	CDA	1.000	0.080	1	20618562	synonymous variant	C/T	snv	0.31	0.34	2
rs11632964	SMAD3	1.000	0.080	15	67071235	intron variant	C/G;T	snv			2
rs201661522	ABCB1	1.000	0.080	7	87539293	missense variant	A/G	snv	6.4E-05	1.0E-04	2
rs7040869		1.000	0.080	9	99072866	downstream gene variant	G/A	snv		0.11	2
rs779179533	TP63	1.000	0.080	3	189808322	missense variant	G/C	snv	4.0E-06		2
rs10898880	LOC107984421 ; ATG16L2	0.925	0.160	11	72814066	upstream gene variant	C/A	snv		0.50	3
rs121913353	BRAF	0.925	0.160	7	140781612	missense variant	C/G;T	snv			3
rs12769316	NFKB2	0.925	0.160	10	102392994	upstream gene variant	G/A	snv		0.13	3
rs41281081	MET	1.000	0.080	7	116796211	3 prime UTR variant	G/A	snv		2.5E-03	3
rs471692	TOP2A	0.925	0.080	17	40400518	intron variant	T/A;C	snv	0.79		3
rs55985569	MET	0.925	0.080	7	116699588	missense variant	G/A;T	snv	3.7E-03		3
rs76322625	MET	1.000	0.080	7	116798111	3 prime UTR variant	C/A;T	snv			3
rs773454677	EGFR	0.925	0.160	7	55205466	missense variant	G/A	snv	1.2E-05		3
rs1564483	BCL2	1.000	0.080	18	63127421	3 prime UTR variant	C/T	snv		0.22	4
rs751306825	ALK	0.925	0.080	2	29220759	missense variant	G/A;T	snv	4.0E-06		4
rs863225283	ALK	0.925	0.080	2	29213993	missense variant	A/C	snv			4
rs1042489	BIRC5	0.851	0.160	17	78224125	3 prime UTR variant	T/C	snv		0.40	5
rs1423493595	UBE2V1 ; TMEM189-UBE2V1	0.851	0.080	20	50082836	missense variant	G/A	snv	4.0E-06	7.0E-06	5
rs1430452530	HIF1A-AS3 ; HIF1A	0.851	0.160	14	61721518	missense variant	A/G	snv	4.0E-06		5
rs759435862	KIDINS220	0.925	0.080	2	8776852	missense variant	C/A;T	snv	2.0E-05		5
rs760943842	ZNF436	0.851	0.080	1	23362976	missense variant	G/A	snv	4.0E-05	1.4E-05	5
rs1057519788	ROS1	0.925	0.080	6	117317184	missense variant	C/T	snv			6
rs121913428	EGFR	0.827	0.120	7	55174015	missense variant	G/A;C	snv			6
rs201744589	TP53	0.882	0.240	17	7673728	stop gained	C/A;G;T	snv	4.0E-06; 1.2E-05		6
rs2131877	XXYLT1	0.827	0.080	3	195137645	intron variant	G/A	snv		0.20	6