DisGeNET - a database of gene-disease associations

List of shared variants

Non-Small Cell Lung Carcinoma, C0007131

Disease: Adenocarcinoma of lung (disorder)

Source: INFERRED ×

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
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
rs104886003	PIK3CA	0.562	0.440	3	179218303	missense variant	G/A;C	snv	4.0E-06		34
rs121913355	BRAF	0.641	0.520	7	140781602	missense variant	C/A;G;T	snv	4.0E-06		32
rs11554290	NRAS	0.583	0.600	1	114713908	missense variant	T/A;C;G	snv			25
rs113488022	BRAF	0.351	0.840	7	140753336	missense variant	A/C;G;T	snv	4.0E-06		22
rs121913273	PIK3CA	0.605	0.440	3	179218294	missense variant	G/A;C	snv			21
rs121913255	NRAS	0.667	0.400	1	114713907	missense variant	T/A;G	snv			19
rs401681	CLPTM1L	0.620	0.640	5	1321972	intron variant	C/T	snv		0.48	17
rs17851045	KRAS	0.672	0.400	12	25227341	missense variant	T/A;G	snv	4.0E-06		15
rs7705526	TERT	0.776	0.240	5	1285859	intron variant	C/A;T	snv			15
rs121913364	BRAF	0.641	0.520	7	140753334	missense variant	T/C;G	snv	4.0E-06		14
rs121913338	BRAF	0.677	0.400	7	140753354	missense variant	T/A;C;G	snv			12
rs121913357	BRAF	0.742	0.320	7	140781603	stop gained	C/A;G;T	snv			11
rs121913530	KRAS	0.583	0.640	12	25245351	missense variant	C/A;G;T	snv			11
rs397516896	BRAF	0.763	0.360	7	140753355	missense variant	C/G;T	snv			11
rs121913351	BRAF	0.776	0.240	7	140781611	missense variant	C/A;G;T	snv	4.0E-06		9
rs121913370	BRAF	0.763	0.360	7	140753393	missense variant	T/C;G	snv			9
rs869025608	MAP2K1	0.763	0.400	15	66435117	missense variant	G/C;T	snv			9
rs56113850	CYP2A6	0.807	0.080	19	40847202	intron variant	T/C	snv		0.52	8
rs55781567	CHRNA5	0.851	0.080	15	78565644	5 prime UTR variant	C/G	snv		0.31	7
rs121913428	EGFR	0.827	0.120	7	55174015	missense variant	G/A;C	snv			4
rs7086803	VTI1A	0.763	0.160	10	112738717	intron variant	G/A	snv		0.20	4
rs11375254	TP63	0.882	0.080	3	189625454	intergenic variant	A/-;AA;AAA;AAAA	delins			3
rs121913444	EGFR	0.724	0.160	7	55191831	missense variant	T/A;C;G	snv			3