DisGeNET - a database of gene-disease associations

List of shared variants

Diabetes Mellitus, Insulin-Dependent, C0011854

Disease: Multiple Sclerosis

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	Num. diseases
rs10735810	VDR	0.662	0.640	12	47879112	start lost	A/C;G;T	snv		26
rs10774671	OAS1	0.732	0.480	12	112919388	splice acceptor variant	G/A;C	snv	0.67	14
rs1267969615	ACE	0.532	0.760	17	63490960	missense variant	T/C	snv	4.0E-06	100
rs12785878	NADSYN1	0.677	0.520	11	71456403	intron variant	G/A;T	snv		25
rs16139	NPY ; LOC107986777	0.658	0.560	7	24285260	missense variant	T/A;C	snv	4.0E-06; 3.0E-02	36
rs17879469	HLA-DRB1	0.763	0.360	6	32584333	missense variant	C/G	snv	1.3E-05	9
rs1805192	PPARG	0.510	0.840	3	12379739	missense variant	C/G	snv		121
rs2041670	CLEC16A	0.851	0.280	16	11080795	intron variant	G/A;C	snv		4
rs2227956	HSPA1L	0.752	0.400	6	31810495	missense variant	G/A;C;T	snv	0.87	12
rs2228570	VDR	0.521	0.760	12	47879112	start lost	A/C;G;T	snv	0.63	99
rs2281808	SIRPG	0.925	0.160	20	1629905	intron variant	T/A;C	snv		4
rs231775	CTLA4	0.504	0.720	2	203867991	missense variant	A/G;T	snv	0.42; 4.0E-06	115
rs241427	TAP2	0.925	0.160	6	32836637	intron variant	A/G;T	snv		2
rs3101942	LOC100294145	0.882	0.200	6	32902280	intergenic variant	G/A;C	snv		3
rs3118470	IL2RA	0.752	0.360	10	6059750	intron variant	T/A;C	snv		10
rs3129941	TSBP1 ; TSBP1-AS1	0.882	0.240	6	32369909	missense variant	A/G;T	snv	0.81	3
rs3134603	PPT2-EGFL8 ; PPT2	0.851	0.360	6	32158225	non coding transcript exon variant	A/C;G;T	snv		4
rs3134943	AGPAT1 ; MIR6833 ; RNF5	0.882	0.240	6	32179984	intron variant	T/A;C	snv	0.89	3
rs3184504	SH2B3 ; ATXN2	0.572	0.600	12	111446804	missense variant	T/A;C;G	snv	0.67	92
rs3775291	TLR3	0.602	0.640	4	186082920	missense variant	C/G;T	snv	1.2E-04; 0.28	51
rs3806156	BTNL2 ; TSBP1-AS1	0.827	0.280	6	32405921	intron variant	G/A;T	snv		5
rs397507444	MTHFR	0.405	0.880	1	11794407	missense variant	T/G	snv		306
rs4746	GLO1	0.708	0.400	6	38682852	missense variant	T/A;G	snv	0.36	21
rs4986790	TLR4	0.438	0.800	9	117713024	missense variant	A/G;T	snv	6.1E-02; 4.0E-06	223
rs5753037	HORMAD2 ; LOC105372988	0.925	0.160	22	30185733	intron variant	C/A;T	snv		2