DisGeNET - a database of gene-disease associations

List of shared variants

Major Depressive Disorder, C1269683

Disease: Attention deficit hyperactivity disorder

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
rs10994359	ANK3	0.827	0.040	10	60462349	intron variant	T/C	snv		8.0E-02	7
rs12966547	LOC105372125	0.827	0.040	18	55084786	intergenic variant	G/A	snv		0.39	7
rs4650608		0.851	0.040	1	78772330	intergenic variant	T/C	snv		0.29	7
rs6323	MAOA	0.807	0.040	X	43731789	synonymous variant	G/T	snv	0.65		7
rs6782011	GRM7	0.807	0.120	3	7457960	intron variant	C/T	snv		0.52	7
rs9275524		0.807	0.160	6	32707332	upstream gene variant	T/C	snv		0.58	7
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
rs9371601	SYNE1	0.790	0.120	6	152469438	intron variant	G/T	snv		0.46	8
rs11191454	LOC107984265 ; BORCS7-ASMT ; AS3MT	0.776	0.160	10	102900247	intron variant	A/G	snv		7.9E-02	9
rs2535629	ITIH3	0.827	0.040	3	52799203	intron variant	G/A;C	snv			9
rs779867	GRM7	0.776	0.120	3	7442784	intron variant	T/C;G	snv			9
rs1480380	HLA-DMB	0.763	0.360	6	32945469	intron variant	C/T	snv		0.11	10
rs3746544	SNAP25 ; SNAP25-AS1	0.790	0.120	20	10306436	3 prime UTR variant	G/T	snv		0.68	10
rs11191580	NT5C2	0.827	0.040	10	103146454	intron variant	T/C	snv		7.9E-02	13
rs1625579	MIR137HG	0.763	0.160	1	98037378	intron variant	G/T	snv		0.78	14
rs6198	NR3C1	0.724	0.480	5	143278056	3 prime UTR variant	T/C	snv		0.12	16
rs8321	ZNRD1	0.742	0.320	6	30064745	3 prime UTR variant	A/C	snv	5.4E-02	5.9E-02	16
rs9296158	FKBP5 ; LOC112267956	0.763	0.080	6	35599305	intron variant	A/G	snv		0.65	16
rs5569	SLC6A2	0.742	0.280	16	55697923	synonymous variant	G/A;C	snv	0.31; 4.0E-06		19
rs1344706	ZNF804A	0.701	0.160	2	184913701	intron variant	A/C;T	snv			21
rs6296	HTR1B ; LOC105377864	0.732	0.160	6	77462543	synonymous variant	C/G	snv	0.31	0.27	23
rs6314	HTR2A	0.677	0.360	13	46834899	missense variant	G/A	snv	7.9E-02	9.5E-02	23
rs4570625	TPH2	0.724	0.200	12	71938143	upstream gene variant	G/T	snv		0.27	25
rs1006737	CACNA1C	0.695	0.120	12	2236129	intron variant	G/A	snv		0.36	27