DisGeNET - a database of gene-disease associations

List of associated variants

Pain, C0030193

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
rs3766246	FAAH			1	46399999	intron variant	A/C;G	snv			2
rs3862188		1.000	0.040	1	247702471	intron variant	T/C	snv		0.44	2
rs5993882	COMT			22	19950010	intron variant	T/C;G	snv			2
rs6473799	OPRK1			8	53240563	intron variant	A/G	snv		0.39	2
rs7734804	LOC105377703			5	164919530	intron variant	G/T	snv		8.3E-02	2
rs806378	CNR1	1.000	0.040	6	88149832	intron variant	C/T	snv		0.21	2
rs9524885	ABCC4			13	95283335	intron variant	T/C	snv		0.63	2
rs11709492	SCN11A			3	38904493	intron variant	C/T	snv		0.26	1
rs11720013	SCN11A			3	38924745	intron variant	G/T	snv		1.0E-01	1
rs11720988	SCN11A			3	38865054	intron variant	G/A	snv		0.26	1
rs11898284	SCN1A-AS1 ; SCN9A			2	166325017	intron variant	A/G	snv		0.15	1
rs11988795	TRPA1 ; MSC-AS1			8	72037366	intron variant	C/G;T	snv			1
rs179971	ATXN1			6	16362511	intron variant	C/T	snv		0.66	1
rs2211843	KCNJ6			21	37811882	intron variant	G/C;T	snv			1
rs2236742	CTSG			14	24575924	intron variant	C/T	snv		0.15	1
rs2756109	ABCC2			10	99798989	intron variant	G/T	snv		0.53	1
rs4512126	ABLIM3			5	149166179	intron variant	T/A;C	snv			1
rs4584690	ABCC4			13	95027878	intron variant	T/C;G	snv			1
rs4587017	UGT2B7			4	69081680	intron variant	T/G	snv		0.63	1
rs6827096	EDNRA			4	147514294	intron variant	C/T	snv		0.30	1
rs7718461	CRHBP			5	76962223	intron variant	A/G	snv		0.51	1
rs7824175	OPRK1			8	53231614	intron variant	C/G;T	snv			1
rs887200	ARVCF			22	19976143	intron variant	C/T	snv		0.74	1
rs941601	SERPINA6			14	94305204	intron variant	C/T	snv		0.19	1
rs8007267		0.882	0.200	14	54912273	intergenic variant	C/T	snv		0.31	6