DisGeNET - a database of gene-disease associations

List of shared variants

Adenocarcinoma of lung (disorder), C0152013

Disease: Primary malignant neoplasm of lung

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
rs104886026	EGFR	0.851	0.080	7	55200333	missense variant	G/A	snv			4
rs425366	CHL1	0.851	0.080	3	283727	intron variant	A/C	snv		0.56	4
rs753273268	NKX2-1 ; NKX2-1-AS1 ; SFTA3	0.851	0.080	14	36520099	missense variant	C/A	snv	4.2E-06		4
rs775439790	CAMK1 ; OGG1	0.851	0.080	3	9765858	missense variant	T/C	snv	8.0E-06	1.4E-05	4
rs9387478	DCBLD1	0.851	0.080	6	117465017	intron variant	C/A;T	snv			4
rs10213865	LOC105374724 ; IL7R	0.827	0.120	5	35857748	intron variant	A/C;T	snv			5
rs1026411	LOC105375751 ; PCAT1	0.827	0.080	8	127014165	intron variant	G/A;C	snv		0.25	5
rs1064607	LPP	0.827	0.200	3	188877884	3 prime UTR variant	G/C	snv		0.46	5
rs1275824108	CDKN3	0.851	0.080	14	54399922	missense variant	A/G	snv		7.0E-06	5
rs2290035	ARNTL	0.827	0.160	11	13386224	intron variant	T/A	snv		0.46	5
rs3733845	CARMN	0.827	0.120	5	149425083	non coding transcript exon variant	G/A	snv		9.3E-02	5
rs4488809	TP63	0.827	0.080	3	189638472	intron variant	T/C	snv		0.45	5
rs4953354	EPAS1	0.827	0.120	2	46348249	intron variant	A/G	snv		0.22	5
rs533748068	ARHGEF2 ; MIR6738	0.851	0.080	1	155950962	missense variant	C/A;T	snv	4.3E-06	7.0E-06	5
rs6790167	TP63	0.827	0.080	3	189869485	intron variant	A/G	snv		0.53	5
rs775057330	CASC1	0.851	0.080	12	25149651	missense variant	C/A;T	snv			5
rs7969931	LRMP	0.851	0.080	12	25089661	missense variant	C/A;G	snv	1.6E-05; 0.75		5
rs2131877	XXYLT1	0.827	0.080	3	195137645	intron variant	G/A	snv		0.20	6
rs2352028	GPC5	0.851	0.080	13	91792975	intron variant	C/G;T	snv			6
rs3733846	CARMN	0.807	0.200	5	149425059	non coding transcript exon variant	T/C	snv		0.19	6
rs3816360	ARNTL	0.807	0.120	11	13346203	intron variant	T/C	snv		0.58	6
rs4513061	AGBL1	0.807	0.080	15	86428401	intron variant	G/A;T	snv			6
rs503464	CHRNA5	0.851	0.080	15	78565554	5 prime UTR variant	T/A	snv		0.28	6
rs595961	AGO1	0.807	0.160	1	35902179	intron variant	A/G	snv	0.30	0.37	6
rs772399455	MYCNOS ; MYCN	0.851	0.080	2	15942096	missense variant	G/A;C	snv	4.0E-06		6