DisGeNET - a database of gene-disease associations

List of shared variants

Major Depressive Disorder, C1269683

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
rs9296158	FKBP5 ; LOC112267956	0.763	0.080	6	35599305	intron variant	A/G	snv		0.65	16
rs6782011	GRM7	0.807	0.120	3	7457960	intron variant	C/T	snv		0.52	7
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
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
rs6296	HTR1B ; LOC105377864	0.732	0.160	6	77462543	synonymous variant	C/G	snv	0.31	0.27	23
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
rs6314	HTR2A	0.677	0.360	13	46834899	missense variant	G/A	snv	7.9E-02	9.5E-02	23
rs2535629	ITIH3	0.827	0.040	3	52799203	intron variant	G/A;C	snv			9
rs12325410	LOC101927026	0.851	0.040	16	9581389	intron variant	T/G	snv		0.16	5
rs12966547	LOC105372125	0.827	0.040	18	55084786	intergenic variant	G/A	snv		0.39	7
rs7004633	LOC105375630	0.851	0.040	8	88748082	intron variant	A/G	snv		0.28	5
rs11191454	LOC107984265 ; BORCS7-ASMT ; AS3MT	0.776	0.160	10	102900247	intron variant	A/G	snv		7.9E-02	9
rs17662626	LOC107985969	0.851	0.040	2	193119895	intergenic variant	A/G	snv		5.9E-02	5
rs6323	MAOA	0.807	0.040	X	43731789	synonymous variant	G/T	snv	0.65		7
rs1625579	MIR137HG	0.763	0.160	1	98037378	intron variant	G/T	snv		0.78	14
rs2721800	MPP6	0.851	0.040	7	24652933	intron variant	G/A;C;T	snv			5
rs1217691063	MTHFR	0.330	0.920	1	11796309	missense variant	A/G	snv	4.0E-06	7.0E-06	614
rs1801133	MTHFR	0.472	0.880	1	11796321	missense variant	G/A	snv	0.31	0.27	174
rs397507444	MTHFR	0.405	0.880	1	11794407	missense variant	T/G	snv			306
rs1805087	MTR	0.496	0.800	1	236885200	missense variant	A/G	snv	0.20	0.21	135
rs3132581	MUCL3 ; HCG21 ; SFTA2	0.851	0.040	6	30945681	intron variant	G/A	snv		9.3E-02	5
rs6198	NR3C1	0.724	0.480	5	143278056	3 prime UTR variant	T/C	snv		0.12	16