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
rs6314	HTR2A	0.677	0.360	13	46834899	missense variant	G/A	snv	7.9E-02	9.5E-02	23
rs10994397	ANK3	0.851	0.040	10	60519366	intron variant	C/T	snv		9.5E-02	5
rs1480380	HLA-DMB	0.763	0.360	6	32945469	intron variant	C/T	snv		0.11	10
rs6198	NR3C1	0.724	0.480	5	143278056	3 prime UTR variant	T/C	snv		0.12	16
rs11178997	TPH2	0.827	0.040	12	71938373	upstream gene variant	T/A	snv		0.12	5
rs6265	BDNF ; BDNF-AS	0.436	0.760	11	27658369	missense variant	C/T	snv	0.19	0.15	272
rs12576775	TENM4	0.827	0.080	11	79366149	intron variant	A/G	snv		0.15	6
rs12325410	LOC101927026	0.851	0.040	16	9581389	intron variant	T/G	snv		0.16	5
rs10503253	CSMD1	0.851	0.040	8	4323322	intron variant	C/A	snv		0.18	5
rs25531	SLC6A4 ; LOC105371720	0.581	0.520	17	30237328	upstream gene variant	T/C	snv		0.18	72
rs2799573	CACNB2	0.851	0.040	10	18312999	intron variant	T/C	snv		0.20	5
rs1805087	MTR	0.496	0.800	1	236885200	missense variant	A/G	snv	0.20	0.21	135
rs2021722	TRIM26	0.851	0.040	6	30206354	intron variant	C/A;T	snv		0.24	5
rs1801260	CLOCK ; TMEM165	0.695	0.280	4	55435202	3 prime UTR variant	A/G	snv		0.25	28
rs1800497	ANKK1	0.620	0.400	11	113400106	missense variant	G/A	snv	0.26	0.26	56
rs6296	HTR1B ; LOC105377864	0.732	0.160	6	77462543	synonymous variant	C/G	snv	0.31	0.27	23
rs1801133	MTHFR	0.472	0.880	1	11796321	missense variant	G/A	snv	0.31	0.27	174
rs4570625	TPH2	0.724	0.200	12	71938143	upstream gene variant	G/T	snv		0.27	25
rs7004633	LOC105375630	0.851	0.040	8	88748082	intron variant	A/G	snv		0.28	5
rs13418455		0.851	0.040	2	180212022	intergenic variant	C/T	snv		0.29	5
rs4650608		0.851	0.040	1	78772330	intergenic variant	T/C	snv		0.29	7
rs1006737	CACNA1C	0.695	0.120	12	2236129	intron variant	G/A	snv		0.36	27
rs11568817	HTR1B ; LOC105377864	0.790	0.120	6	77463665	5 prime UTR variant	A/C	snv		0.37	8
rs13072940		0.851	0.040	3	36801132	regulatory region variant	T/A	snv		0.37	5
rs12966547	LOC105372125	0.827	0.040	18	55084786	intergenic variant	G/A	snv		0.39	7