DisGeNET - a database of gene-disease associations

List of shared variants

Neoplasms, C0027651

Disease: Malignant neoplasm of colon and/or rectum

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 GENOME	Num. diseases
rs10090154		0.807	0.160	8	127519892	intergenic variant	T/A;C	snv		7
rs10165970	NPAS2	0.708	0.320	2	100840527	intron variant	G/A	snv	0.16	18
rs10519097	RORA	0.708	0.320	15	60997989	intron variant	C/T	snv	0.13	18
rs1056836	CYP1B1	0.581	0.680	2	38071060	missense variant	G/C	snv	0.51	58
rs1057519860	EGFR	0.851	0.080	7	55160316	missense variant	C/A	snv		5
rs1057519943	POLE	0.790	0.160	12	132676598	missense variant	G/C;T	snv		10
rs1060503115	PMS2	0.763	0.400	7	5978664	missense variant	T/A;G	snv		13
rs1064795841	TP53	0.882	0.080	17	7674971	missense variant	C/T	snv		4
rs10795668	LOC105376400	0.724	0.160	10	8659256	upstream gene variant	G/A	snv	0.24	17
rs10889677	IL23R	0.627	0.720	1	67259437	3 prime UTR variant	C/A	snv	0.27	40
rs112445441	KRAS	0.658	0.400	12	25245347	missense variant	C/A;G;T	snv		32
rs1131691014	TP53	0.439	0.800	17	7676154	frameshift variant	-/C	ins		214
rs1143623	IL1B	0.677	0.440	2	112838252	upstream gene variant	C/G	snv	0.24	29
rs11943456	TMEM165	0.708	0.320	4	55410167	intron variant	T/C	snv	0.42	18
rs121913227	BRAF	0.653	0.320	7	140753336	missense variant	AC/CT;TT	mnv		31
rs121913238	KRAS	0.732	0.240	12	25227343	missense variant	G/C;T	snv		17
rs121913254	NRAS	0.658	0.440	1	114713909	stop gained	G/A;C;T	snv		31
rs121913338	BRAF	0.677	0.400	7	140753354	missense variant	T/A;C;G	snv		24
rs121913377	BRAF	0.354	0.840	7	140753335	missense variant	CA/AT;TT	mnv		480
rs121913530	KRAS	0.583	0.640	12	25245351	missense variant	C/A;G;T	snv		63
rs1230416942	TTI2 ; MAK16	0.925	0.080	8	33498547	missense variant	G/C	snv	7.0E-06	3
rs12733285	ADIPOR1	0.776	0.120	1	202952912	intron variant	C/T	snv	0.26	12
rs1342387	ADIPOR1	0.776	0.120	1	202945228	intron variant	T/C	snv	0.53	12
rs1447295	CASC8	0.658	0.400	8	127472793	intron variant	A/C;T	snv		29
rs145204276	ZBTB37 ; SNORD74 ; SNORD75 ; GAS5 ; SNORD77 ; SNORA103 ; SNORD76	0.658	0.320	1	173868254	splice donor variant	CAAGG/-	delins	8.8E-02	31