DisGeNET - a database of gene-disease associations

List of associated variants

Epstein-Barr Virus Infections, C0149678

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
rs2395185	HLA-DRB9	0.724	0.360	6	32465390	intron variant	G/T	snv		0.29	17
rs9268853	HLA-DRB9	0.790	0.440	6	32461866	intron variant	T/C	snv		0.29	10
rs2239804	HLA-DRA	0.851	0.240	6	32443746	intron variant	T/A;C	snv	0.51		5
rs2239802	HLA-DRA	0.882	0.200	6	32444069	intron variant	C/A;G;T	snv			4
rs2239803	HLA-DRA	0.882	0.240	6	32444056	intron variant	C/A;T	snv		0.50	4
rs3129888	HLA-DRA	0.882	0.240	6	32443949	intron variant	G/A	snv	0.82	0.80	4
rs12759054	SLC35F3	1.000	0.040	1	233984064	intron variant	T/A;C	snv			3
rs2294881	BTNL2 ; TSBP1-AS1	1.000	0.040	6	32399827	intron variant	T/C	snv		0.19	3
rs3130048	BAG6	1.000	0.120	6	31645962	intron variant	T/C	snv		0.23	3
rs2294882	TSBP1-AS1 ; BTNL2			6	32399738	intron variant	T/C	snv		0.19	2
rs2736157	MIR6832 ; PRRC2A	1.000	0.120	6	31633043	intron variant	A/G;T	snv	0.15	0.17	2
rs4248166	TSBP1-AS1 ; BTNL2	1.000	0.040	6	32398644	intron variant	T/C	snv		0.18	2
rs4935356	HLA-DRA	1.000	0.080	6	32444611	intron variant	T/A;G	snv			2
rs9268658	HLA-DRA	1.000	0.040	6	32442939	intron variant	G/A;C	snv			2
rs1161098	LOC105369812 ; LINC02408			12	67453680	intron variant	G/A	snv		0.84	1
rs116671518	DKK2			4	107189709	intron variant	T/C	snv		1.9E-02	1
rs204992	PBX2			6	32189131	intron variant	G/A	snv		0.22	1
rs2153486				14	87737048	intron variant	C/T	snv		0.68	1
rs2294884	TSBP1-AS1 ; BTNL2			6	32399482	intron variant	T/A;G	snv		0.18	1
rs3104369	HLA-DQA1			6	32634705	intron variant	T/C	snv		0.71	1
rs3130070	PRRC2A			6	31624031	intron variant	A/G	snv		0.17	1
rs3130623	PRRC2A			6	31629923	intron variant	C/T	snv		0.18	1
rs594418	NRG3			10	82625296	intron variant	G/A	snv		0.83	1
rs6105452	MACROD2			20	15683126	intron variant	C/T	snv		0.10	1
rs62309385				4	136134743	intron variant	G/C	snv		9.8E-02	1