DisGeNET - a database of gene-disease associations

List of associated variants

Colorectal Carcinoma, C0009402

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
rs200936057	ZZEF1 ; CYB5D2	1.000	0.080	17	4143774	missense variant	C/G;T	snv	4.8E-05; 2.4E-05		1
rs145011101	ZSCAN5A	1.000	0.080	19	56223783	missense variant	C/G;T	snv	9.5E-05; 4.0E-05		1
rs750071607	ZSCAN16 ; ZSCAN16-AS1	1.000	0.080	6	28126805	missense variant	G/A	snv	2.2E-05		1
rs369664812	ZNHIT1	1.000	0.080	7	101223799	missense variant	C/T	snv	2.8E-05	4.2E-05	1
rs12646351	ZNF827	0.790	0.080	4	145819473	intron variant	G/A	snv		0.19	10
rs17806780	ZNF827	0.790	0.080	4	145811502	intron variant	T/C	snv		0.18	10
rs13230517	ZNF727	1.000	0.080	7	64076947	intron variant	A/G	snv		0.65	1
rs10414971	ZNF442	1.000	0.080	19	12351131	missense variant	G/A	snv	1.9E-03	7.8E-03	1
rs757755988	ZNF442	1.000	0.080	19	12350857	missense variant	C/G;T	snv	6.0E-05; 4.0E-06		1
rs200399581	ZNF43	1.000	0.080	19	21809307	missense variant	G/A	snv	1.8E-04	2.0E-04	1
rs757067821	ZNF385D	1.000	0.080	3	21421246	missense variant	C/A;T	snv	4.0E-06; 4.0E-06		1
rs1338565	ZNF239	1.000	0.080	10	43564228	intron variant	C/A;G	snv			1
rs767530299	ZNF217	1.000	0.080	20	53581860	missense variant	C/T	snv	4.0E-06	7.0E-06	1
rs3826392	ZNF18 ; MAP2K4	0.827	0.200	17	12019587	intron variant	G/T	snv		0.65	5
rs191217255	ZMYM4	1.000	0.080	1	35415633	missense variant	C/T	snv	2.0E-05	7.0E-06	1
rs704017	ZMIZ1-AS1	0.776	0.080	10	79059375	intron variant	A/G	snv		0.55	10
rs1250567	ZMIZ1	0.776	0.080	10	79286508	intron variant	T/C	snv		0.56	10
rs12373	ZG16B	0.925	0.080	16	2832196	3 prime UTR variant	G/T	snv	0.66	0.63	2
rs568589179	ZDHHC2	1.000	0.080	8	17217176	missense variant	G/C	snv			1
rs145204276	ZBTB37 ; SNORD74 ; SNORD75 ; GAS5 ; SNORD77 ; SNORA103 ; SNORD76	0.658	0.320	1	173868254	splice donor variant	CAAGG/-	delins		8.8E-02	31
rs10511330	ZBTB20	0.776	0.080	3	114402172	intron variant	T/C	snv		0.22	10
rs3747093	YDJC	0.732	0.200	22	21630090	upstream gene variant	G/A	snv		0.32	16
rs11685387	XRCC5	0.776	0.240	2	216109091	splice region variant	C/T	snv		0.30	9
rs9288518	XRCC5	0.776	0.240	2	216196997	intron variant	A/G	snv		0.35	9
rs6869366	XRCC4 ; TMEM167A	0.701	0.280	5	83075927	intron variant	T/G	snv		9.2E-02	18