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
rs4105144		0.827	0.160	19	40852719	intron variant	T/C	snv			7
rs4324798		0.790	0.240	6	28808340	intergenic variant	G/A	snv		7.2E-02	8
rs4975616		0.763	0.320	5	1315545	downstream gene variant	G/A	snv		0.51	12
rs4513061	AGBL1	0.807	0.080	15	86428401	intron variant	G/A;T	snv			6
rs595961	AGO1	0.807	0.160	1	35902179	intron variant	A/G	snv	0.30	0.37	6
rs1057519784	ALK	0.827	0.080	2	29220765	missense variant	G/T	snv			7
rs1130409	APEX1	0.555	0.720	14	20456995	missense variant	T/A;C;G	snv	4.0E-06; 4.0E-06; 0.42		72
rs533748068	ARHGEF2 ; MIR6738	0.851	0.080	1	155950962	missense variant	C/A;T	snv	4.3E-06	7.0E-06	5
rs2290035	ARNTL	0.827	0.160	11	13386224	intron variant	T/A	snv		0.46	5
rs3816360	ARNTL	0.807	0.120	11	13346203	intron variant	T/C	snv		0.58	6
rs189037	ATM ; NPAT	0.689	0.400	11	108223106	5 prime UTR variant	G/A	snv		0.49	22
rs3117582	BAG6 ; APOM	0.716	0.440	6	31652743	intron variant	T/G	snv		7.1E-02	14
rs113488022	BRAF	0.351	0.840	7	140753336	missense variant	A/C;G;T	snv	4.0E-06		490
rs121913377	BRAF	0.354	0.840	7	140753335	missense variant	CA/AT;TT	mnv			480
rs11571833	BRCA2	0.608	0.360	13	32398489	stop gained	A/T	snv	6.6E-03	6.0E-03	43
rs775439790	CAMK1 ; OGG1	0.851	0.080	3	9765858	missense variant	T/C	snv	8.0E-06	1.4E-05	4
rs3733845	CARMN	0.827	0.120	5	149425083	non coding transcript exon variant	G/A	snv		9.3E-02	5
rs3733846	CARMN	0.807	0.200	5	149425059	non coding transcript exon variant	T/C	snv		0.19	6
rs775057330	CASC1	0.851	0.080	12	25149651	missense variant	C/A;T	snv			5
rs735482	CD3EAP ; ERCC1	0.742	0.160	19	45408744	missense variant	A/C	snv	0.21	0.20	16
rs1535045	CD40	0.742	0.360	20	46119460	intron variant	C/A;G;T	snv			12
rs2151280	CDKN2B-AS1	0.701	0.360	9	22034720	non coding transcript exon variant	G/A	snv		0.46	16
rs1444669684	CDKN2B-AS1 ; CDKN2A	0.658	0.480	9	21994285	missense variant	C/A;T	snv			36
rs1275824108	CDKN3	0.851	0.080	14	54399922	missense variant	A/G	snv		7.0E-06	5
rs425366	CHL1	0.851	0.080	3	283727	intron variant	A/C	snv		0.56	4