DisGeNET - a database of gene-disease associations

List of associated variants

Addictive Behavior, C0085281

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
rs113488022	BRAF	0.351	0.840	7	140753336	missense variant	A/C;G;T	snv	4.0E-06		490
rs121913377	BRAF	0.354	0.840	7	140753335	missense variant	CA/AT;TT	mnv			480
rs6265	BDNF ; BDNF-AS	0.436	0.760	11	27658369	missense variant	C/T	snv	0.19	0.15	272
rs4680	COMT ; MIR4761	0.442	0.920	22	19963748	missense variant	G/A	snv	0.46	0.44	249
rs759834365	BDNF-AS ; BDNF	0.448	0.760	11	27658456	missense variant	C/T	snv	1.2E-05		237
rs1799971	OPRM1	0.559	0.600	6	154039662	missense variant	A/G	snv	0.19	0.12	95
rs1800497	ANKK1	0.620	0.400	11	113400106	missense variant	G/A	snv	0.26	0.26	56
rs324420	FAAH	0.637	0.440	1	46405089	missense variant	C/A	snv	0.24	0.26	48
rs1049353	CNR1	0.630	0.600	6	88143916	synonymous variant	C/T	snv	0.21	0.20	42
rs6277	DRD2	0.689	0.480	11	113412737	synonymous variant	G/A	snv	0.41	0.38	36
rs1333048	CDKN2B-AS1	0.683	0.320	9	22125348	intron variant	A/C	snv		0.44	24
rs2023239	CNR1	0.724	0.160	6	88150763	intron variant	T/C	snv		0.21	20
rs1044396	CHRNA4	0.742	0.240	20	63349782	missense variant	G/A;C	snv	0.47; 6.1E-05		17
rs1611115	DBH	0.732	0.280	9	133635393	upstream gene variant	T/C	snv		0.80	16
rs1333045	CDKN2B-AS1	0.776	0.280	9	22119196	non coding transcript exon variant	T/C	snv		0.50	14
rs1803274	BCHE	0.763	0.360	3	165773492	missense variant	C/T	snv	0.18	0.18	13
rs2283265	DRD2	0.776	0.160	11	113414814	intron variant	C/A	snv		0.16	12
rs796065354	ESR1	0.882	0.080	6	151944320	missense variant	A/G	snv			9
rs769540300	OPRM1	0.851	0.200	6	154091047	missense variant	G/A	snv	1.2E-05		8
rs2251214	SYT1	0.827	0.040	12	79430071	intron variant	A/G;T	snv			7
rs774847933	COMT ; MIR4761	0.882	0.200	22	19962797	missense variant	A/G	snv	8.0E-06		5
rs75012854	MIR4761 ; COMT	0.882	0.200	22	19962641	missense variant	A/G	snv		7.0E-06	5
rs678849	OPRD1	0.882	0.120	1	28818676	intron variant	C/T	snv		0.44	5
rs751416416	OPRK1	0.882	0.120	8	53250920	missense variant	C/A;T	snv	8.3E-06; 4.1E-06		5
rs2070762	TH	0.925	0.080	11	2165105	intron variant	A/G	snv		0.43	5