DisGeNET - a database of gene-disease associations

List of associated variants

Encephalitis, C0014038

Source: ALL

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
rs1800872	IL19 ; IL10	0.495	0.840	1	206773062	5 prime UTR variant	T/G	snv		0.69	119
rs1800871	IL19 ; IL10	0.508	0.800	1	206773289	5 prime UTR variant	A/G	snv		0.69	108
rs763780	IL17F	0.531	0.720	6	52236941	missense variant	T/C	snv	6.7E-02	6.6E-02	87
rs34637584	LRRK2	0.583	0.480	12	40340400	missense variant	G/A	snv	5.3E-04	3.6E-04	78
rs1556620697	SH2D1A ; STAG2	0.827	0.360	X	124365758	splice region variant	C/G	snv			10
rs1799821	CPT2	0.827	0.200	1	53210776	missense variant	G/A	snv	0.49	0.46	8
rs2229291	CPT2	0.827	0.200	1	53210729	missense variant	T/G	snv	2.3E-02	1.5E-02	8
rs1557055311	ABCD1	0.882	0.200	X	153743220	splice acceptor variant	G/A;C	snv			5
rs1799822	CPT2	0.925	0.080	1	53213557	missense variant	A/G	snv	0.16	0.15	4
rs2858870	HLA-DRB1	0.851	0.280	6	32604474	intergenic variant	T/A;C	snv			4
rs2227283	GRIK2	0.882	0.080	6	102055442	missense variant	G/A;C;T	snv	0.40; 4.0E-06		3
rs1889570	IL17F	0.882	0.160	6	52245936	upstream gene variant	C/A;T	snv			3
rs2227288	CD320	1.000	0.040	19	8302641	intron variant	G/C;T	snv	0.12	0.14	2
rs1010930015	TBK1	1.000	0.040	12	64460250	missense variant	A/C	snv	4.2E-06		2
rs1555202947	TBK1	1.000	0.040	12	64467018	missense variant	G/C	snv			2
rs739901	OAS2	1.000	0.040	12	112977858	intron variant	C/A	snv		0.18	1
rs35311343	TLR3	1.000	0.040	4	186082575	missense variant	C/G	snv	1.5E-03	1.6E-03	1
rs753482575	TLR3	1.000	0.040	4	186078995	missense variant	A/T	snv	8.0E-06	2.8E-05	1