DisGeNET - a database of gene-disease associations

List of associated variants

Malignant neoplasm of lung, C0242379

Source: ALL

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
rs2281089	IL2RB	0.851	0.200	22	37136132	intron variant	A/G	snv		0.17	4
rs11090910	MIRLET7A3 ; MIRLET7BHG ; MIR4763 ; MIRLET7B	0.882	0.080	22	46111790	non coding transcript exon variant	T/C	snv		0.30	3
rs11703832	MIRLET7BHG	0.882	0.080	22	46108287	intron variant	C/T	snv		0.19	3
rs12170325	MIRLET7BHG	0.882	0.080	22	46106990	intron variant	C/T	snv		0.18	3
rs13053856	MIRLET7BHG	0.882	0.080	22	46104002	intron variant	G/A;T	snv			3
rs2236141	CHEK2 ; HSCB	0.882	0.080	22	28741882	5 prime UTR variant	C/T	snv		0.10	3
rs2267029	MMP11	0.882	0.080	22	23775729	intron variant	A/G	snv		0.92	3
rs5756523		0.882	0.080	22	37117508	intergenic variant	T/A;C	snv			3
rs663048	SEZ6L	0.882	0.080	22	26299111	missense variant	G/A;T	snv	4.2E-06; 0.19		3
rs745794582	CYP2D6 ; NDUFA6-DT ; LOC112268294	0.882	0.080	22	42130751	missense variant	G/A	snv	4.5E-06		3
rs746764639	MIR4761 ; COMT	0.882	0.080	22	19962714	missense variant	T/C	snv	2.4E-05	3.5E-05	3
rs750269833	CYP2D6 ; NDUFA6-DT ; LOC112268294	0.882	0.080	22	42129119	missense variant	C/T	snv	4.1E-06		3
rs876659871	CHEK2	0.882	0.080	22	28719462	missense variant	C/T	snv		7.0E-06	3
rs9614159	LOC105372988 ; HORMAD2	0.882	0.160	22	30205254	intron variant	G/A	snv		0.30	3
rs2051764	MTMR3	0.925	0.080	22	29965892	intron variant	G/A;C	snv		0.74	2
rs36605	MTMR3	0.925	0.080	22	29944367	intron variant	A/G;T	snv			2
rs718772	HORMAD2	0.925	0.120	22	30108218	intron variant	A/C;G	snv			2
rs737909	MTMR3	0.925	0.080	22	29992769	non coding transcript exon variant	T/G	snv		0.73	2
rs11090598	HORMAD2	1.000	0.080	22	30125781	intron variant	A/G	snv		0.21	1
rs12167333	HORMAD2	1.000	0.080	22	30179823	downstream gene variant	C/T	snv		0.21	1
rs193473	HORMAD2-AS1	1.000	0.080	22	30052410	intron variant	A/G;T	snv			1
rs1978083	HORMAD2	1.000	0.080	22	30174454	intron variant	C/G	snv		0.21	1
rs200426271	MTMR3	1.000	0.080	22	29948468	intron variant	-/G	ins			1
rs2017677	MTMR3	1.000	0.080	22	29987273	non coding transcript exon variant	G/C;T	snv			1
rs2023683	LOC105372988 ; HORMAD2	1.000	0.080	22	30203607	intron variant	G/A	snv		0.22	1