DisGeNET - a database of gene-disease associations

List of associated variants

Malignant neoplasm of colon and/or rectum, C4722085

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 EXOME	AF GENOME	Num. diseases
rs373001	MIR301B ; MIR130B	0.925	0.080	22	21653137	intron variant	C/G;T	snv			2
rs1466012753	MLH1	0.925	0.080	3	37014525	synonymous variant	C/T	snv	4.0E-06		2
rs28756992	MLH3	0.925	0.080	14	75047123	missense variant	T/C	snv	1.1E-02	1.5E-02	2
rs755990134	MMP2	0.925	0.080	16	55489730	synonymous variant	C/T	snv	3.2E-05	7.0E-06	2
rs1215486792	MOK	0.925	0.080	14	102229572	missense variant	C/G	snv		7.0E-06	2
rs780178752	MSH2	0.925	0.080	2	47403350	synonymous variant	C/T	snv	4.3E-06	1.4E-05	2
rs4659744	MTR	0.925	0.080	1	236896158	intron variant	G/C	snv		0.34	2
rs587782041	MUTYH	0.925	0.080	1	45333297	missense variant	G/A;T	snv	6.0E-05	7.0E-06	2
rs5995355	NCF4-AS1	0.925	0.080	22	36855419	intron variant	A/G;T	snv			2
rs2282151	NFKBIE ; SLC35B2	0.925	0.080	6	44258458	3 prime UTR variant	T/C	snv		0.17	2
rs67491583	PCAT1 ; POU5F1B ; CCAT2 ; CASC8	0.925	0.080	8	127401984	non coding transcript exon variant	GA/-	delins			2
rs141178472	PIK3CA	0.925	0.080	3	179234393	3 prime UTR variant	T/C	snv	3.0E-03	3.3E-03	2
rs1052748	PLD2	0.925	0.080	17	4817174	missense variant	C/T	snv	0.39	0.36	2
rs767449295	POLD1	0.925	0.080	19	50402669	missense variant	C/T	snv	1.7E-05	2.8E-05	2
rs780865223	POLE	0.925	0.080	12	132672754	missense variant	T/C	snv	1.2E-05	1.2E-04	2
rs980578884	POLE	0.925	0.080	12	132673217	missense variant	C/T	snv		1.4E-05	2
rs9858822	PPARG	0.925	0.080	3	12369739	intron variant	A/C	snv		0.11	2
rs3774921	PPARGC1A	0.925	0.080	4	23809024	intron variant	C/T	snv		0.55	2
rs714775	SCARNA10 ; NCAPD2	0.925	0.080	12	6510236	non coding transcript exon variant	T/A;C	snv	1.0E-03; 0.18		2
rs1725459	SIPA1L3	0.925	0.080	19	38049092	intron variant	C/A;G;T	snv			2
rs867538330	SLCO6A1	0.925	0.080	5	102458457	synonymous variant	C/T	snv			2
rs118049207	SND1	0.925	0.080	7	127890817	intron variant	A/G	snv		1.7E-03	2
rs3755457	TACR1	0.925	0.080	2	75064383	intron variant	G/A	snv		0.28	2
rs3757417	TPST1	0.925	0.080	7	66360270	3 prime UTR variant	T/C;G	snv		9.0E-02	2
rs750248338	TYMS ; ENOSF1	0.925	0.080	18	670857	missense variant	C/T	snv	4.0E-06		2