DisGeNET - a database of gene-disease associations

List of associated variants

Alcohol Use Disorder, C0001956

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
rs17777298	LOC107986462 ; HTR4	1.000	0.080	5	148541962	intron variant	T/A	snv		0.24	1
rs2074957	PIP5K1C	1.000	0.080	19	3653527	synonymous variant	C/A;T	snv	8.0E-06; 0.57		1
rs4432372	PIP5K1C	1.000	0.080	19	3698844	intron variant	A/G;T	snv			1
rs4807493	PIP5K1C	1.000	0.080	19	3631038	3 prime UTR variant	A/G	snv		0.84	1
rs6990313	GATA4	1.000	0.080	8	11712527	intron variant	G/T	snv		0.14	1
rs8109485	PIP5K1C	1.000	0.080	19	3664096	intron variant	A/G	snv		0.21	1
rs916264	APOL2	1.000	0.080	22	36237790	intron variant	A/C;T	snv			1
rs110402	CRHR1 ; LINC02210-CRHR1 ; MAPT-AS1	0.790	0.120	17	45802681	intron variant	G/A;C	snv			12
rs10112596	GATA4	0.925	0.120	8	11722293	intron variant	A/G	snv		0.83	3
rs2412646	CLOCK ; TMEM165	0.882	0.120	4	55452605	3 prime UTR variant	T/C	snv		0.58	3
rs4532	DRD1	0.827	0.160	5	175443147	5 prime UTR variant	C/T	snv	0.68	0.72	7
rs17153694	GATA4	0.851	0.160	8	11730972	intron variant	C/T	snv		0.12	4
rs356200	SNCA	0.882	0.160	4	89747463	intron variant	T/C	snv		0.44	4
rs1015443	PRH1-PRR4 ; PRR4 ; TAS2R13 ; PRH1	0.925	0.160	12	10908523	missense variant	T/A;C	snv	4.0E-06; 0.59		2
rs6971	TSPO	0.742	0.200	22	43162920	missense variant	A/G	snv	0.76	0.75	11
rs7958822	ARNTL2	0.807	0.200	12	27348173	intron variant	G/A	snv		0.43	6
rs6923761	GLP1R	0.851	0.200	6	39066296	missense variant	G/A;C	snv	0.23; 4.0E-06		4
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
rs53576	OXTR ; CAV3	0.641	0.320	3	8762685	intron variant	A/G;T	snv			42
rs324981	NPSR1-AS1 ; NPSR1	0.724	0.320	7	34778501	missense variant	A/T	snv	0.44	0.47	18
rs6318	HTR2C ; LOC105373313	0.623	0.520	X	114731326	missense variant	C/G;T	snv			42
rs1229984	ADH1B	0.570	0.560	4	99318162	missense variant	T/C;G	snv	0.90		83
rs1799971	OPRM1	0.559	0.600	6	154039662	missense variant	A/G	snv	0.19	0.12	95
rs696217	GHRL ; GHRLOS	0.662	0.640	3	10289773	missense variant	G/T	snv	8.8E-02	7.1E-02	32