DisGeNET - a database of gene-disease associations

List of associated variants

Substance Use Disorders, C0038586

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
rs4680	COMT ; MIR4761	0.442	0.920	22	19963748	missense variant	G/A	snv	0.46	0.44	249
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
rs6277	DRD2	0.689	0.480	11	113412737	synonymous variant	G/A	snv	0.41	0.38	36
rs9296158	FKBP5 ; LOC112267956	0.763	0.080	6	35599305	intron variant	A/G	snv		0.65	16
rs1076560	DRD2	0.776	0.120	11	113412966	intron variant	C/A	snv		0.16	11
rs11568817	HTR1B ; LOC105377864	0.790	0.120	6	77463665	5 prime UTR variant	A/C	snv		0.37	8
rs130058	HTR1B ; LOC105377864	0.790	0.120	6	77463564	5 prime UTR variant	T/A;G	snv			8
rs7794745	CNTNAP2	0.851	0.040	7	146792514	intron variant	A/T	snv		0.49	6
rs1843809	TPH2	0.851	0.080	12	71954918	intron variant	G/T	snv		0.77	6
rs373611092	MIR4761 ; COMT	0.925	0.160	22	19962794	missense variant	A/G	snv	8.4E-05	4.9E-05	5
rs6565113	CDH13	0.925	0.040	16	83074041	intron variant	G/C;T	snv			3
rs2519152	DBH	1.000	0.040	9	133644512	intron variant	T/C	snv		0.40	2
rs2402959	LOC105375501			7	129765967	intron variant	A/G	snv		0.26	1
rs6965643	LOC105375501			7	129767724	intron variant	A/G	snv		0.28	1