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
rs6694545		0.851	0.040	1	29964421	intergenic variant	A/G	snv		0.58	5
rs8321	ZNRD1	0.742	0.320	6	30064745	3 prime UTR variant	A/C	snv	5.4E-02	5.9E-02	16
rs2021722	TRIM26	0.851	0.040	6	30206354	intron variant	C/A;T	snv		0.24	5
rs25531	SLC6A4 ; LOC105371720	0.581	0.520	17	30237328	upstream gene variant	T/C	snv		0.18	72
rs3132581	MUCL3 ; HCG21 ; SFTA2	0.851	0.040	6	30945681	intron variant	G/A	snv		9.3E-02	5
rs9275524		0.807	0.160	6	32707332	upstream gene variant	T/C	snv		0.58	7
rs1480380	HLA-DMB	0.763	0.360	6	32945469	intron variant	C/T	snv		0.11	10
rs9296158	FKBP5 ; LOC112267956	0.763	0.080	6	35599305	intron variant	A/G	snv		0.65	16
rs1360780	FKBP5 ; LOC112267956	0.708	0.320	6	35639794	intron variant	T/A;C	snv			31
rs9394309	FKBP5	0.851	0.040	6	35654004	intron variant	G/A	snv		0.74	4
rs13072940		0.851	0.040	3	36801132	regulatory region variant	T/A	snv		0.37	5
rs10503253	CSMD1	0.851	0.040	8	4323322	intron variant	C/A	snv		0.18	5
rs6323	MAOA	0.807	0.040	X	43731789	synonymous variant	G/T	snv	0.65		7
rs6314	HTR2A	0.677	0.360	13	46834899	missense variant	G/A	snv	7.9E-02	9.5E-02	23
rs6313	HTR2A	0.562	0.640	13	46895805	synonymous variant	G/A	snv	0.41	0.40	82
rs6311	HTR2A	0.645	0.640	13	46897343	upstream gene variant	C/T	snv		0.40	41
rs1715	ZNF615	0.851	0.040	19	51991525	3 prime UTR variant	T/C	snv		1.4E-05	5
rs2535629	ITIH3	0.827	0.040	3	52799203	intron variant	G/A;C	snv			9
rs12966547	LOC105372125	0.827	0.040	18	55084786	intergenic variant	G/A	snv		0.39	7
rs9951150		0.851	0.040	18	55153893	intergenic variant	A/G;T	snv			5
rs11152369	TCF4	0.851	0.040	18	55399097	intron variant	A/C	snv		6.3E-02	5
rs1801260	CLOCK ; TMEM165	0.695	0.280	4	55435202	3 prime UTR variant	A/G	snv		0.25	28
rs28386840		0.827	0.080	16	55652906	upstream gene variant	T/A;C	snv			6
rs5569	SLC6A2	0.742	0.280	16	55697923	synonymous variant	G/A;C	snv	0.31; 4.0E-06		19
rs10994359	ANK3	0.827	0.040	10	60462349	intron variant	T/C	snv		8.0E-02	7