DisGeNET - a database of gene-disease associations

List of shared variants

Adenocarcinoma of lung (disorder), C0152013

Disease: Malignant neoplasm of lung

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
rs1051730	CHRNA3	0.641	0.600	15	78601997	synonymous variant	G/A	snv	0.27	0.26	11
rs10519198	IREB2	0.925	0.080	15	78450412	intron variant	C/A;G	snv			2
rs1062980	IREB2	0.827	0.080	15	78500185	3 prime UTR variant	T/C	snv		0.39	6
rs11571833	BRCA2	0.608	0.360	13	32398489	stop gained	A/T	snv	6.6E-03	6.0E-03	21
rs11638372	LOC112268142 ; CHRNB4	0.925	0.080	15	78691217	intron variant	C/A;G;T	snv		0.28	5
rs1235162	GABBR1	0.827	0.280	6	29569447	intron variant	A/G	snv		6.0E-02	6
rs12441998	CHRNB4	0.925	0.080	15	78637030	intron variant	G/A	snv		0.63	3
rs12594247	CHRNB4	0.925	0.080	15	78654291	intron variant	C/T	snv		0.14	3
rs1270942	CFB ; CYP21A2	0.742	0.440	6	31951083	non coding transcript exon variant	A/G	snv		7.5E-02	7
rs12910984	CHRNA3	0.827	0.080	15	78599285	intron variant	G/A;C;T	snv			4
rs12914385	CHRNA3	0.790	0.160	15	78606381	intron variant	C/A;T	snv			13
rs1316971	CHRNB4	0.925	0.080	15	78638168	intron variant	A/G;T	snv		0.62	3
rs13180	IREB2	0.851	0.160	15	78497146	synonymous variant	C/T	snv	0.54	0.51	6
rs13314271	TP63	0.925	0.080	3	189639813	intron variant	T/C	snv		0.45	2
rs1394371		0.925	0.080	15	78432127	intergenic variant	C/T	snv		0.22	4
rs17487514	CHRNB4 ; LOC112268142 ; RPL18P11	0.925	0.080	15	78661443	non coding transcript exon variant	C/T	snv		0.19	3
rs1794282		0.807	0.320	6	32698749	intergenic variant	C/T	snv		6.4E-02	6
rs2036534	HYKK	0.827	0.080	15	78534606	3 prime UTR variant	T/C	snv		0.26	5
rs2187668	LOC107986589 ; HLA-DQA2 ; HLA-DQA1	0.701	0.480	6	32638107	intron variant	C/T	snv		3.3E-03	18
rs2256543	HLA-A	0.925	0.080	6	29970056	downstream gene variant	T/C	snv		0.59	2
rs2523987	TRIM31-AS1 ; TRIM31	0.827	0.280	6	30112216	intron variant	A/C	snv		9.2E-02	5
rs259919	ZNRD1ASP	0.882	0.080	6	30057726	intron variant	G/A	snv		0.25	6
rs259940	ZNRD1ASP	0.925	0.080	6	30044157	intron variant	A/G	snv		0.23	2
rs2656069	IREB2	0.882	0.080	15	78453365	intron variant	C/G;T	snv			4
rs2734986	LOC105375010	0.827	0.160	6	29850791	intron variant	T/C	snv		0.10	3