DisGeNET - a database of gene-disease associations

List of shared variants

Squamous cell carcinoma of lung, C0149782

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
rs144594252	DDR2	0.882	0.080	1	162754625	missense variant	C/G	snv	6.8E-05	5.6E-05	3
rs1057519847	EGFR	0.570	0.560	7	55191821	missense variant	CT/AG	mnv			72
rs1057519848	EGFR	0.570	0.560	7	55191822	missense variant	TG/GT	mnv			72
rs121434568	EGFR	0.568	0.560	7	55191822	missense variant	T/A;G	snv			73
rs121913428	EGFR	0.827	0.120	7	55174015	missense variant	G/A;C	snv			6
rs121913444	EGFR	0.724	0.160	7	55191831	missense variant	T/A;C;G	snv			18
rs150036236	EGFR	0.925	0.080	7	55191741	missense variant	G/A	snv	4.8E-05	3.5E-05	3
rs397517097	EGFR	0.851	0.080	7	55174777	missense variant	T/C	snv			4
rs121913465	EGFR ; EGFR-AS1	0.763	0.160	7	55181312	missense variant	G/T	snv			11
rs1057519895	FBXW7	0.724	0.240	4	152328232	missense variant	C/A;G;T	snv			17
rs867384286	FBXW7	0.732	0.240	4	152328233	missense variant	G/A;C	snv	4.3E-06		14
rs11200014	FGFR2	0.695	0.280	10	121575416	intron variant	G/A;T	snv		0.34	19
rs121913482	FGFR3	0.630	0.680	4	1801837	missense variant	C/T	snv			45
rs56084662	FRY	0.701	0.280	13	32295727	3 prime UTR variant	G/A	snv		3.5E-03	18
rs56404467	FRY	0.708	0.280	13	32265853	intron variant	G/A	snv		1.3E-02	17
rs1057941	GBAP1	0.701	0.280	1	155216951	non coding transcript exon variant	G/A;T	snv	0.46		18
rs115392158	HLA-B	0.708	0.280	6	31347004	intron variant	A/G	snv			17
rs12601991	HNF1B	0.708	0.280	17	37741642	intron variant	T/A;G	snv			17
rs121913233	HRAS ; LRRC56	0.627	0.520	11	533874	missense variant	T/A;C;G	snv			37
rs11119608	KCNH1	0.708	0.280	1	210816167	intron variant	T/G	snv		0.21	17
rs121913530	KRAS	0.583	0.640	12	25245351	missense variant	C/A;G;T	snv			63
rs17851045	KRAS	0.672	0.400	12	25227341	missense variant	T/A;G	snv	4.0E-06		27
rs73110464	KRT8	0.708	0.280	12	52918828	intron variant	C/T	snv		0.12	17
rs3813565	LOC105370913 ; CHRNB4	0.851	0.080	15	78727268	splice region variant	G/A;T	snv			6
rs75316749	LOC107986051	0.701	0.280	3	169043635	intergenic variant	A/G	snv		4.2E-02	18