DisGeNET - a database of gene-disease associations

List of shared variants

Carcinoma of lung, C0684249

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
rs11703832	MIRLET7BHG	0.882	0.080	22	46108287	intron variant	C/T	snv		0.19	3
rs11715541	FEZF2 ; LOC105377647	0.882	0.080	3	62373795	intron variant	G/T	snv			3
rs1174612410	SLC12A9	0.882	0.080	7	100860016	missense variant	A/G	snv	4.0E-06	7.0E-06	3
rs117781739		0.882	0.080	16	47835114	intron variant	G/A;T	snv			3
rs118137916	IL7R	0.882	0.080	5	35863436	intron variant	A/C;G	snv			3
rs11853991	TGM5	0.882	0.080	15	43265351	intron variant	A/G;T	snv			3
rs11878644		0.882	0.080	19	45373709	upstream gene variant	T/C	snv		0.53	3
rs1196929947	ERBB2	0.882	0.080	17	39723351	missense variant	G/A	snv			3
rs12050604	UBR1	0.882	0.080	15	43065208	intron variant	A/C;T	snv			3
rs12170325	MIRLET7BHG	0.882	0.080	22	46106990	intron variant	C/T	snv		0.18	3
rs1221157259	RB1	0.882	0.080	13	48453069	missense variant	C/T	snv	4.0E-06		3
rs12212247	FGFR1OP	0.882	0.080	6	167000051	non coding transcript exon variant	T/C	snv	0.38	0.35	3
rs12333226	LOC100129636	0.882	0.080	6	29042166	intron variant	A/T	snv		6.2E-02	3
rs1246463849	PRRC2A	0.882	0.080	6	31624466	missense variant	C/T	snv	8.0E-06		3
rs12536544	RAC1	0.882	0.080	7	6396270	intron variant	G/A	snv		0.23	3
rs1255722	PPP2R5E ; LOC112268140	0.882	0.080	14	63544119	non coding transcript exon variant	A/G	snv		0.45	3
rs12569923	IL2RA	0.882	0.080	10	6042690	intron variant	C/G;T	snv			3
rs12571445	ERCC6	0.882	0.080	10	49514137	intron variant	A/G	snv		7.0E-03	3
rs12722498	IL2RA	0.882	0.080	10	6053873	intron variant	A/G	snv		4.3E-02	3
rs12828	MAF ; WWOX	0.882	0.080	16	79212426	3 prime UTR variant	G/A;C	snv			3
rs13009079	CIR1 ; SCRN3	0.882	0.080	2	174396420	intron variant	T/C	snv		0.26	3
rs13032404	COL6A3	0.882	0.080	2	237324840	intron variant	G/A	snv	0.29	0.26	3
rs13053856	MIRLET7BHG	0.882	0.080	22	46104002	intron variant	G/A;T	snv			3
rs1305755801	TP53BP2	0.882	0.080	1	223802799	missense variant	G/A;T	snv	8.0E-06; 4.0E-06		3
rs13073869	PPARG	0.882	0.080	3	12312494	intron variant	G/A;C	snv			3