DisGeNET - a database of gene-disease associations

List of associated variants

Cholangitis, Sclerosing, C0008313

Source: GWASCAT ×

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
rs35736272	ZPBP2	0.807	0.160	17	39876427	intron variant	T/C	snv		0.35	5
rs259964	ZNF831	0.827	0.120	20	59249254	intron variant	A/G;T	snv			6
rs10761648	ZNF365	0.827	0.120	10	62594503	intron variant	C/T	snv		0.20	5
rs7915475	ZNF365	0.827	0.120	10	62621908	intron variant	A/G	snv		0.28	5
rs1250573	ZMIZ1	0.827	0.120	10	79282718	intron variant	G/A	snv		0.23	5
rs140135	ZMAT5 ; UQCR10	0.827	0.120	22	29767846	non coding transcript exon variant	C/G	snv		0.79	5
rs4143332	ZDHHC20P2	1.000	0.040	6	31380588	non coding transcript exon variant	G/A	snv		8.2E-02	1
rs2266961	UBE2L3	0.807	0.160	22	21574308	intron variant	C/G	snv		0.18	6
rs1893592	UBASH3A	0.742	0.280	21	42434957	missense variant	A/C;G	snv	0.27; 8.0E-06		7
rs12720356	TYK2	0.752	0.360	19	10359299	missense variant	A/C;G	snv	6.1E-02; 4.0E-06		7
rs35018800	TYK2	0.790	0.160	19	10354167	missense variant	G/A	snv	4.6E-03	4.9E-03	5
rs7097656	TSPAN14	0.827	0.120	10	80491075	intron variant	T/C;G	snv			6
rs74817271	TNIP1	0.807	0.120	5	151090412	intron variant	G/A	snv		5.0E-02	6
rs7848647	TNFSF15	0.732	0.320	9	114806766	upstream gene variant	T/C	snv		0.74	6
rs6062496	TNFRSF6B ; RTEL1-TNFRSF6B	0.827	0.120	20	63697746	intron variant	G/A	snv		0.52	6
rs1860545	TNFRSF1A	0.790	0.200	12	6337611	intron variant	G/A	snv		0.31	5
rs2234161	TNFRSF14	0.827	0.120	1	2559766	non coding transcript exon variant	C/T	snv	4.1E-05; 0.55	0.58	5
rs582757	TNFAIP3	0.776	0.320	6	137876687	intron variant	C/T	snv		0.70	5
rs4986790	TLR4	0.438	0.800	9	117713024	missense variant	A/G;T	snv	6.1E-02; 4.0E-06		6
rs77981966	THADA	0.827	0.120	2	43550825	intron variant	C/T	snv		4.6E-02	5
rs11691685	TEX41	0.827	0.120	2	144724260	intron variant	A/G	snv		5.2E-02	5
rs1452787	TCF4	0.827	0.160	18	55539976	intron variant	A/G	snv		0.24	2
rs79390277	TANGO6	1.000	0.040	16	68908687	intron variant	A/C	snv		3.6E-02	1
rs72977586	STK11	0.827	0.120	19	1186317	intron variant	G/C	snv		0.16	5
rs12942547	STAT3	0.807	0.200	17	42375526	intron variant	A/G;T	snv			6