DisGeNET - a database of gene-disease associations

List of shared variants

Primary malignant neoplasm of lung, C1306460

Disease: Adenocarcinoma of lung (disorder)

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
rs1131691014	TP53	0.439	0.800	17	7676154	frameshift variant	-/C	ins			214
rs425366	CHL1	0.851	0.080	3	283727	intron variant	A/C	snv		0.56	4
rs735482	CD3EAP ; ERCC1	0.742	0.160	19	45408744	missense variant	A/C	snv	0.21	0.20	16
rs1057519975	TP53	0.649	0.480	17	7675209	missense variant	A/C;G;T	snv			34
rs113488022	BRAF	0.351	0.840	7	140753336	missense variant	A/C;G;T	snv	4.0E-06		490
rs760043106	TP53	0.645	0.440	17	7674947	missense variant	A/C;G;T	snv			32
rs10213865	LOC105374724 ; IL7R	0.827	0.120	5	35857748	intron variant	A/C;T	snv			5
rs6505162	NSRP1 ; MIR3184 ; MIR423	0.695	0.320	17	30117165	5 prime UTR variant	A/C;T	snv	0.50; 3.1E-05		25
rs7041	GC	0.576	0.800	4	71752617	missense variant	A/C;T	snv	0.52; 4.0E-06		64
rs1136410	PARP1	0.559	0.760	1	226367601	missense variant	A/G	snv	0.21	0.15	70
rs1217691063	MTHFR	0.330	0.920	1	11796309	missense variant	A/G	snv	4.0E-06	7.0E-06	614
rs1275824108	CDKN3	0.851	0.080	14	54399922	missense variant	A/G	snv		7.0E-06	5
rs4953354	EPAS1	0.827	0.120	2	46348249	intron variant	A/G	snv		0.22	5
rs595961	AGO1	0.807	0.160	1	35902179	intron variant	A/G	snv	0.30	0.37	6
rs6790167	TP63	0.827	0.080	3	189869485	intron variant	A/G	snv		0.53	5
rs8042374	CHRNA3	0.807	0.200	15	78615690	intron variant	A/G	snv		0.29	10
rs859	STARD5 ; IL16	0.807	0.200	15	81308981	3 prime UTR variant	A/G	snv		0.33	6
rs876658657	MLH1	0.677	0.280	3	37020356	missense variant	A/G	snv	4.0E-06		25
rs121913279	PIK3CA	0.526	0.560	3	179234297	missense variant	A/G;T	snv	4.0E-06; 4.0E-06		101
rs5275	PTGS2	0.583	0.560	1	186673926	3 prime UTR variant	A/G;T	snv			55
rs11571833	BRCA2	0.608	0.360	13	32398489	stop gained	A/T	snv	6.6E-03	6.0E-03	43
rs397517132	EGFR	0.623	0.280	7	55191846	missense variant	A/T	snv			48
rs2073498	RASSF1	0.763	0.280	3	50332115	missense variant	C/A	snv	9.6E-02	8.0E-02	12
rs2736100	TERT	0.550	0.880	5	1286401	3 prime UTR variant	C/A	snv		0.52	83
rs31489	CLPTM1L	0.763	0.320	5	1342599	intron variant	C/A	snv		0.41	10