DisGeNET - a database of gene-disease associations

List of associated variants

Alcohol Use Disorder, C0001956

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
rs56013859	PER2	0.925	0.080	2	238276865	intron variant	T/C	snv		0.11	2
rs53576	OXTR ; CAV3	0.641	0.320	3	8762685	intron variant	A/G;T	snv			42
rs696217	GHRL ; GHRLOS	0.662	0.640	3	10289773	missense variant	G/T	snv	8.8E-02	7.1E-02	32
rs1229984	ADH1B	0.570	0.560	4	99318162	missense variant	T/C;G	snv	0.90		83
rs698	ADH1C ; ADH1B	0.724	0.240	4	99339632	missense variant	T/A;C	snv	0.35		20
rs356219	LOC105377329 ; SNCA	0.776	0.240	4	89716450	intron variant	G/A	snv		0.54	9
rs279858	GABRA2	0.851	0.080	4	46312576	synonymous variant	T/C	snv	0.40	0.38	8
rs2066702	ADH1B	0.882	0.080	4	99307860	missense variant	G/A	snv	1.5E-02	5.9E-02	7
rs279871	GABRA2	0.882	0.080	4	46303716	intron variant	T/C	snv		0.38	5
rs356200	SNCA	0.882	0.160	4	89747463	intron variant	T/C	snv		0.44	4
rs2412646	CLOCK ; TMEM165	0.882	0.120	4	55452605	3 prime UTR variant	T/C	snv		0.58	3
rs11240	CLOCK ; TMEM165	0.925	0.080	4	55453183	3 prime UTR variant	C/A;G	snv			2
rs11941860	GABRG1	1.000	0.080	4	46080161	intron variant	C/T	snv		0.12	2
rs2119183	GABRA2	1.000	0.080	4	46270789	intron variant	G/A	snv		7.6E-02	2
rs3756007	GABRA2	1.000	0.080	4	46389047	5 prime UTR variant	T/C	snv		5.4E-02	2
rs536599		1.000	0.080	4	46196917	intergenic variant	G/T	snv		0.47	2
rs141973904	ADH1B ; ADH1C	1.000	0.080	4	99341085	intron variant	C/T	snv		1.6E-02	1
rs2910164	MIR3142HG ; MIR146A	0.447	0.880	5	160485411	mature miRNA variant	C/G	snv	0.71; 4.1E-06	0.70	193
rs4532	DRD1	0.827	0.160	5	175443147	5 prime UTR variant	C/T	snv	0.68	0.72	7
rs463379	SLC6A3	0.882	0.080	5	1431049	intron variant	G/C	snv		0.31	3
rs6350	SLC6A3	0.882	0.080	5	1443084	missense variant	G/A;C	snv	5.6E-02; 6.8E-05		3
rs3811939	CRHBP	1.000	0.080	5	76954762	intron variant	G/A	snv		0.27	2
rs10044881	HTR4	1.000	0.080	5	148645656	non coding transcript exon variant	T/C	snv		0.17	1
rs17777298	LOC107986462 ; HTR4	1.000	0.080	5	148541962	intron variant	T/A	snv		0.24	1
rs1799971	OPRM1	0.559	0.600	6	154039662	missense variant	A/G	snv	0.19	0.12	95