DisGeNET - a database of gene-disease associations

List of shared variants

Bipolar Disorder, C0005586

Disease: Attention deficit hyperactivity disorder

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
rs10489744	RXRG	0.925	0.040	1	165411386	intron variant	G/A	snv		0.55	2
rs11162556		0.925	0.040	1	78795698	intergenic variant	A/G	snv		0.32	2
rs1217691063	MTHFR	0.330	0.920	1	11796309	missense variant	A/G	snv	4.0E-06	7.0E-06	614
rs1625579	MIR137HG	0.763	0.160	1	98037378	intron variant	G/T	snv		0.78	14
rs1801131	MTHFR	0.535	0.840	1	11794419	missense variant	T/G	snv	0.29	0.26	93
rs1801133	MTHFR	0.472	0.880	1	11796321	missense variant	G/A	snv	0.31	0.27	174
rs1805087	MTR	0.496	0.800	1	236885200	missense variant	A/G	snv	0.20	0.21	135
rs2252865	RERE	0.851	0.040	1	8362616	intron variant	T/C	snv		0.72	6
rs397507444	MTHFR	0.405	0.880	1	11794407	missense variant	T/G	snv			306
rs4650608		0.851	0.040	1	78772330	intergenic variant	T/C	snv		0.29	7
rs6675281	DISC2 ; DISC1 ; TSNAX-DISC1 ; LOC105373170	0.827	0.080	1	231818355	missense variant	C/T	snv	0.11	0.14	7
rs6694545		0.851	0.040	1	29964421	intergenic variant	A/G	snv		0.58	5
rs13418455		0.851	0.040	2	180212022	intergenic variant	C/T	snv		0.29	5
rs1344706	ZNF804A	0.701	0.160	2	184913701	intron variant	A/C;T	snv			21
rs17662626	LOC107985969	0.851	0.040	2	193119895	intergenic variant	A/G	snv		5.9E-02	5
rs3749034	GAD1	0.827	0.040	2	170816965	5 prime UTR variant	G/A;T	snv			6
rs3771829	TACR1	0.790	0.120	2	75137019	intron variant	C/G	snv		0.11	9
rs3771856	TACR1 ; LOC105374811 ; LOC105374812	0.882	0.080	2	75186888	non coding transcript exon variant	G/A	snv		0.57	3
rs56037433	SLC4A10	0.925	0.040	2	161719475	intron variant	G/A;T	snv			2
rs71420669	LOC105376755	0.925	0.040	2	194986941	intergenic variant	C/A	snv		6.6E-02	2
rs13061878	PTPRG	0.925	0.040	3	61634560	intron variant	A/T	snv		9.7E-02	2
rs13072940		0.851	0.040	3	36801132	regulatory region variant	T/A	snv		0.37	5
rs2535629	ITIH3	0.827	0.040	3	52799203	intron variant	G/A;C	snv			9
rs34096808	NLGN1	0.925	0.040	3	173822316	intron variant	C/T	snv		3.1E-02	2
rs6280	DRD3	0.602	0.520	3	114171968	missense variant	C/T	snv	0.63	0.54	57