DisGeNET - a database of gene-disease associations

List of shared variants

Colorectal Carcinoma, C0009402

Disease: 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
rs3733845	CARMN	0.827	0.120	5	149425083	non coding transcript exon variant	G/A	snv		9.3E-02	5
rs9912300	ACLY	0.827	0.120	17	41869011	intron variant	G/A;C;T	snv	4.2E-06; 0.78		5
rs3733846	CARMN	0.807	0.200	5	149425059	non coding transcript exon variant	T/C	snv		0.19	6
rs3814058	NR1I2	0.851	0.120	3	119818444	3 prime UTR variant	T/C	snv		0.28	6
rs376040996	XPA	0.790	0.120	9	97687210	missense variant	T/C;G	snv	1.2E-05; 2.0E-05		7
rs768873896	MTHFR	0.790	0.160	1	11794822	missense variant	C/G;T	snv	8.0E-06; 2.4E-05		7
rs751763046	EXO1	0.790	0.200	1	241885375	missense variant	T/C	snv	4.0E-06		8
rs2069514		0.807	0.160	15	74745879	upstream gene variant	G/A	snv		0.13	9
rs7086803	VTI1A	0.763	0.160	10	112738717	intron variant	G/A	snv		0.20	9
rs7727691	XRCC4 ; TMEM167A	0.763	0.200	5	83075876	intron variant	C/T	snv		0.32	9
rs7904519	TCF7L2	0.763	0.240	10	113014168	intron variant	A/G	snv		0.55	9
rs10680577	RAB4B-EGLN2 ; EGLN2	0.776	0.160	19	40798690	intron variant	-/TACT	delins			10
rs11196067	VTI1A	0.752	0.160	10	112709306	intron variant	A/T	snv		0.32	10
rs369410616	MUTYH	0.752	0.280	1	45329400	missense variant	C/T	snv	2.0E-05	2.8E-05	10
rs4809957	CYP24A1	0.763	0.240	20	54154632	3 prime UTR variant	A/G	snv		0.29	10
rs760025060	CYP1B1 ; CYP1B1-AS1	0.776	0.200	2	38074936	missense variant	C/T	snv			10
rs1105879	UGT1A9 ; UGT1A6 ; UGT1A7 ; UGT1A10 ; UGT1A8	0.790	0.240	2	233693556	missense variant	A/C	snv	0.35	0.34	11
rs213210	MIR219A1 ; RING1	0.742	0.240	6	33208047	upstream gene variant	A/C;G	snv			11
rs7025417	LOC107987046 ; IL33	0.752	0.280	9	6240084	intron variant	T/C;G	snv			11
rs941759532	ERCC4	0.763	0.240	16	13932175	missense variant	C/G	snv			11
rs2470890	CYP1A2	0.742	0.320	15	74755085	synonymous variant	T/C	snv		0.57	12
rs3757441	EZH2	0.752	0.200	7	148827660	intron variant	C/T	snv		0.80	12
rs6068816	CYP24A1	0.752	0.200	20	54164552	synonymous variant	C/T	snv	0.12	8.9E-02	12
rs2075686	TMEM167A ; XRCC4	0.742	0.240	5	83076927	intron variant	C/T	snv		1.7E-02	13
rs2808630		0.742	0.240	1	159711078	downstream gene variant	C/T	snv		0.77	13