DisGeNET - a database of gene-disease associations

Source: GWASDB

Variants associated to the Disease: Crohn Disease ×

Variants associated to the Gene: IL23R ×

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
rs11209026	IL23R	0.597	0.680	1	67240275	missense variant	G/A	snv	4.2E-02	4.6E-02	5
rs2201841	C1orf141 ; IL23R	0.716	0.440	1	67228519	intron variant	A/G;T	snv			4
rs11465804	IL23R	0.752	0.320	1	67236843	intron variant	T/G	snv	4.4E-02	5.4E-02	3
rs10889677	IL23R	0.627	0.720	1	67259437	3 prime UTR variant	C/A	snv		0.27	2
rs9988642	IL23R	0.882	0.080	1	67260421	downstream gene variant	T/C	snv		0.13	2
rs7517847	IL23R ; C1orf141	0.689	0.600	1	67215986	intron variant	T/G	snv		0.37	2
rs1004819	C1orf141 ; IL23R	0.776	0.360	1	67204530	intron variant	G/A	snv		0.30	1
rs11805303	C1orf141 ; IL23R	0.827	0.240	1	67209833	intron variant	C/T	snv		0.30	1
rs2064689	C1orf141 ; IL23R	1.000	0.040	1	67187327	intron variant	G/A	snv		0.29	1
rs7539625	C1orf141 ; IL23R	1.000	0.040	1	67207082	intron variant	G/A	snv	0.33	0.30	1
rs10889676	IL23R	0.827	0.120	1	67256884	intron variant	C/A;T	snv			1
rs11804284	IL23R	1.000	0.040	1	67233571	intron variant	T/A;C;G	snv			1
rs1343151	IL23R	0.752	0.400	1	67253446	intron variant	G/A	snv		0.41	1
rs10489629	IL23R ; C1orf141	0.827	0.240	1	67222666	intron variant	T/C	snv		0.48	1
rs11209008	IL23R ; C1orf141	0.882	0.080	1	67157615	intron variant	G/A;T	snv		5.7E-02	1
rs11465802	IL23R ; C1orf141	1.000	0.040	1	67219915	intron variant	A/C;T	snv			1
rs2902440	IL23R ; C1orf141	1.000	0.040	1	67205233	intron variant	G/A	snv		0.37	1
rs7518660	IL23R ; C1orf141	0.925	0.120	1	67219760	intron variant	G/A	snv	0.43	0.47	1
rs76418789	IL23R ; C1orf141	0.882	0.080	1	67182913	missense variant	G/A	snv	7.3E-03	4.5E-03	1