DisGeNET - a database of gene-disease associations

List of shared variants

Diabetes Mellitus, Insulin-Dependent, C0011854

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
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
rs11580078	C1orf141 ; IL23R	0.724	0.240	1	67203951	intron variant	C/A;G	snv			14
rs1217691063	MTHFR	0.330	0.920	1	11796309	missense variant	A/G	snv	4.0E-06	7.0E-06	614
rs2066363	ADGRL2	0.724	0.240	1	81771892	intron variant	C/T	snv		0.71	14
rs2476601	AP4B1-AS1 ; PTPN22	0.498	0.800	1	113834946	missense variant	A/G	snv	0.93	0.93	121
rs3024493	IL19 ; IL10	0.776	0.280	1	206770623	intron variant	C/A;T	snv		0.11	9
rs34884278		0.724	0.240	1	172869708	intron variant	C/T	snv		0.63	14
rs3789604	RSBN1 ; AP4B1-AS1	0.776	0.360	1	113812320	synonymous variant	T/A;C;G	snv	8.5E-06; 1.3E-05; 0.17		9
rs397507444	MTHFR	0.405	0.880	1	11794407	missense variant	T/G	snv			306
rs55705316		0.724	0.240	1	206760172	regulatory region variant	T/A;G	snv			14
rs6679677	PHTF1	0.653	0.320	1	113761186	upstream gene variant	C/A	snv		6.7E-02	26
rs6689858	CRB1	0.724	0.240	1	197406337	intron variant	T/C	snv		0.39	14
rs114846446	LINC01250	0.724	0.240	2	2944140	intron variant	G/A	snv		9.5E-03	14
rs1260326	GCKR	0.645	0.600	2	27508073	missense variant	T/C;G	snv	0.63; 4.0E-06	0.68	81
rs1990760	IFIH1	0.672	0.480	2	162267541	missense variant	C/T	snv	0.50	0.45	33
rs2075184		0.724	0.240	2	102464132	intergenic variant	T/C	snv		0.78	14
rs2111485		0.724	0.280	2	162254026	regulatory region variant	A/G	snv		0.46	17
rs35667974	IFIH1	0.776	0.280	2	162268127	missense variant	T/C	snv	1.1E-02	1.2E-02	9
rs36001488	ATG16L1	0.724	0.240	2	233276621	intron variant	C/T	snv		0.44	14
rs3747517	IFIH1	0.732	0.360	2	162272314	missense variant	T/C	snv	0.68	0.68	13
rs4676410	GPR35	0.716	0.240	2	240624322	intron variant	G/A	snv		0.26	17
rs7574865	STAT4	0.574	0.720	2	191099907	intron variant	T/G	snv		0.79	59
rs4625	DAG1	0.716	0.280	3	49534707	3 prime UTR variant	A/G	snv		0.30	17
rs2069762	IL2	0.672	0.560	4	122456825	upstream gene variant	A/C	snv		0.24	23