DisGeNET - a database of gene-disease associations

List of shared variants

Attention deficit hyperactivity disorder, C1263846

Disease: Mental disorders

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
rs1344706	ZNF804A	0.701	0.160	2	184913701	intron variant	A/C;T	snv			21
rs4570625	TPH2	0.724	0.200	12	71938143	upstream gene variant	G/T	snv		0.27	25
rs3771829	TACR1	0.790	0.120	2	75137019	intron variant	C/G	snv		0.11	9
rs25531	SLC6A4 ; LOC105371720	0.581	0.520	17	30237328	upstream gene variant	T/C	snv		0.18	72
rs7341475	RELN	0.851	0.240	7	103764368	intron variant	G/A	snv		0.17	6
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
rs1217691063	MTHFR	0.330	0.920	1	11796309	missense variant	A/G	snv	4.0E-06	7.0E-06	614
rs397507444	MTHFR	0.405	0.880	1	11794407	missense variant	T/G	snv			306
rs11789399	LOC105376249	0.882	0.040	9	118597008	intergenic variant	G/A;C	snv			5
rs736707	LOC101927870 ; RELN	0.851	0.040	7	103489956	intron variant	A/G	snv		0.30	6
rs4916723	LINC00461	0.925	0.040	5	88558577	intron variant	A/C;G;T	snv			4
rs2535629	ITIH3	0.827	0.040	3	52799203	intron variant	G/A;C	snv			9
rs6318	HTR2C ; LOC105373313	0.623	0.520	X	114731326	missense variant	C/G;T	snv			42
rs6311	HTR2A	0.645	0.640	13	46897343	upstream gene variant	C/T	snv		0.40	41
rs6313	HTR2A	0.562	0.640	13	46895805	synonymous variant	G/A	snv	0.41	0.40	82
rs6296	HTR1B ; LOC105377864	0.732	0.160	6	77462543	synonymous variant	C/G	snv	0.31	0.27	23
rs1360780	FKBP5 ; LOC112267956	0.708	0.320	6	35639794	intron variant	T/A;C	snv			31
rs9296158	FKBP5 ; LOC112267956	0.763	0.080	6	35599305	intron variant	A/G	snv		0.65	16
rs9470080	FKBP5	0.827	0.080	6	35678658	intron variant	T/A;C	snv			13
rs6280	DRD3	0.602	0.520	3	114171968	missense variant	C/T	snv	0.63	0.54	57
rs1801028	DRD2	0.716	0.200	11	113412762	missense variant	G/C	snv	2.7E-02	1.8E-02	24
rs4680	COMT ; MIR4761	0.442	0.920	22	19963748	missense variant	G/A	snv	0.46	0.44	249
rs2254298	CAV3 ; OXTR	0.701	0.200	3	8760542	intron variant	G/A	snv		0.16	23
rs1006737	CACNA1C	0.695	0.120	12	2236129	intron variant	G/A	snv		0.36	27