DisGeNET - a database of gene-disease associations

List of shared variants

Crohn Disease, C0010346

Disease: Psoriasis

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
rs1061622	TNFRSF1B	0.633	0.760	1	12192898	missense variant	T/G	snv	0.22	0.22	33
rs10800314		0.827	0.120	1	161502999	upstream gene variant	C/A	snv		0.65	5
rs10889676	IL23R	0.827	0.120	1	67256884	intron variant	C/A;T	snv			5
rs10889677	IL23R	0.627	0.720	1	67259437	3 prime UTR variant	C/A	snv		0.27	40
rs11209026	IL23R	0.597	0.680	1	67240275	missense variant	G/A	snv	4.2E-02	4.6E-02	46
rs11209032		0.752	0.400	1	67274409	upstream gene variant	G/A	snv		0.30	10
rs114202211	HIPK1	0.827	0.120	1	113943285	intron variant	T/C	snv		8.1E-03	5
rs11465804	IL23R	0.752	0.320	1	67236843	intron variant	T/G	snv	4.4E-02	5.4E-02	10
rs11580078	C1orf141 ; IL23R	0.724	0.240	1	67203951	intron variant	C/A;G	snv			14
rs11805303	C1orf141 ; IL23R	0.827	0.240	1	67209833	intron variant	C/T	snv		0.30	6
rs12075255	IL19	0.827	0.120	1	206788283	intron variant	A/G	snv		0.74	5
rs12131796	INAVA	0.827	0.120	1	200909599	intron variant	G/A	snv		0.22	5
rs1217691063	MTHFR	0.330	0.920	1	11796309	missense variant	A/G	snv	4.0E-06	7.0E-06	614
rs1333062	ITLN1	0.807	0.200	1	160876494	downstream gene variant	T/C;G	snv			6
rs1343151	IL23R	0.752	0.400	1	67253446	intron variant	G/A	snv		0.41	10
rs16841904	DENND1B	0.807	0.160	1	197732862	intron variant	C/T	snv		0.18	6
rs1800871	IL19 ; IL10	0.508	0.800	1	206773289	5 prime UTR variant	A/G	snv		0.69	108
rs1800896	IL19 ; IL10	0.507	0.800	1	206773552	intron variant	T/C	snv		0.41	113
rs183686347	IL23R	0.827	0.120	1	67237759	intron variant	G/A	snv		4.8E-03	5
rs2066363	ADGRL2	0.724	0.240	1	81771892	intron variant	C/T	snv		0.71	14
rs2201841	C1orf141 ; IL23R	0.716	0.440	1	67228519	intron variant	A/G;T	snv			14
rs2234161	TNFRSF14	0.827	0.120	1	2559766	non coding transcript exon variant	C/T	snv	4.1E-05; 0.55	0.58	5
rs2476601	AP4B1-AS1 ; PTPN22	0.498	0.800	1	113834946	missense variant	A/G	snv	0.93	0.93	121
rs2816958	NR5A2	0.827	0.120	1	200132792	intron variant	A/G	snv		0.84	6
rs3024493	IL19 ; IL10	0.776	0.280	1	206770623	intron variant	C/A;T	snv		0.11	9