DisGeNET - a database of gene-disease associations

List of shared variants

Primary malignant neoplasm of lung, C1306460

Disease: Colorectal Carcinoma

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 GENOME	Num. diseases
rs10505477	CASC8 ; PCAT1 ; POU5F1B	0.658	0.400	8	127395198	intron variant	A/G	snv	0.40	31
rs10506868	VTI1A	0.716	0.160	10	112559621	intron variant	C/T	snv	3.1E-02	16
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
rs11196172	TCF7L2	0.708	0.200	10	112967084	intron variant	G/A	snv	0.13	18
rs11568820	VDR	0.672	0.480	12	47908762	intron variant	C/T	snv	0.38	27
rs12241008	VTI1A	0.716	0.160	10	112520943	intron variant	T/C	snv	0.13	16
rs12255372	TCF7L2	0.667	0.480	10	113049143	intron variant	G/A;T	snv		28
rs1447295	CASC8	0.658	0.400	8	127472793	intron variant	A/C;T	snv		29
rs1800469	B9D2 ; TGFB1	0.547	0.760	19	41354391	intron variant	A/G	snv	0.69	78
rs1800896	IL19 ; IL10	0.507	0.800	1	206773552	intron variant	T/C	snv	0.41	113
rs2075686	TMEM167A ; XRCC4	0.742	0.240	5	83076927	intron variant	C/T	snv	1.7E-02	13
rs2267437	DESI1 ; XRCC6	0.724	0.320	22	41620695	intron variant	C/A;G	snv		19
rs2279744	MDM2	0.605	0.640	12	68808800	intron variant	T/G	snv	0.31	48
rs2298881	ERCC1	0.653	0.400	19	45423658	intron variant	C/A;T	snv		25
rs28360071	XRCC4	0.708	0.240	5	83142293	intron variant	GATGAGGAAACTAACTCTCAGTGGTGTTTA/-	delins	0.48	18
rs28360317	XRCC4	0.716	0.280	5	83323739	intron variant	-/CCT	delins	0.24	15
rs3757441	EZH2	0.752	0.200	7	148827660	intron variant	C/T	snv	0.80	12
rs3813867	LOC107984284 ; CYP2E1	0.732	0.240	10	133526101	intron variant	G/A;C	snv		13
rs6721961	NFE2L2	0.672	0.520	2	177265309	intron variant	T/C;G	snv	0.89	24
rs6869366	XRCC4 ; TMEM167A	0.701	0.280	5	83075927	intron variant	T/G	snv	9.2E-02	18
rs7025417	LOC107987046 ; IL33	0.752	0.280	9	6240084	intron variant	T/C;G	snv		11
rs7086803	VTI1A	0.763	0.160	10	112738717	intron variant	G/A	snv	0.20	9
rs762551	CYP1A2	0.701	0.400	15	74749576	intron variant	C/A	snv	0.67	23
rs7727691	XRCC4 ; TMEM167A	0.763	0.200	5	83075876	intron variant	C/T	snv	0.32	9