DisGeNET - a database of gene-disease associations

List of shared variants

Bipolar Disorder, C0005586

Disease: Unipolar Depression

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
rs1006737	CACNA1C	0.695	0.120	12	2236129	intron variant	G/A	snv		0.36	27
rs10405744	ZNF93	0.851	0.040	19	19948684	intron variant	G/A	snv		9.0E-02	4
rs1045642	ABCB1	0.456	0.840	7	87509329	synonymous variant	A/G;T	snv	0.50		214
rs1049353	CNR1	0.630	0.600	6	88143916	synonymous variant	C/T	snv	0.21	0.20	42
rs10494251	BCL9	0.851	0.040	1	147552120	intron variant	C/T	snv		5.8E-02	4
rs10968749	LINGO2	0.851	0.040	9	28752486	intergenic variant	A/G	snv		5.5E-02	4
rs10994336	ANK3	0.776	0.160	10	60420054	intron variant	C/T	snv		7.5E-02	12
rs11030101	BDNF-AS ; BDNF	0.763	0.160	11	27659197	5 prime UTR variant	A/T	snv		0.36	10
rs1176744	HTR3B	0.708	0.240	11	113932306	missense variant	A/C	snv	0.33	0.36	19
rs11829119	LOC107984527	0.851	0.040	12	19040597	intergenic variant	T/A;C	snv			4
rs1217691063	MTHFR	0.330	0.920	1	11796309	missense variant	A/G	snv	4.0E-06	7.0E-06	614
rs12476147	ZNF804A	0.851	0.040	2	184936178	missense variant	A/T	snv	0.66	0.59	4
rs12649507	CLOCK	0.851	0.080	4	55514317	intron variant	G/A;T	snv			4
rs1344706	ZNF804A	0.701	0.160	2	184913701	intron variant	A/C;T	snv			21
rs135745		0.763	0.200	22	38287631	downstream gene variant	G/C	snv		0.48	13
rs139459337	ZBTB20	0.882	0.040	3	114997018	intron variant	C/T	snv		4.7E-02	3
rs140504	LOC107985554 ; BCR	0.882	0.040	22	23285182	missense variant	A/G	snv	0.81	0.86	3
rs1541187	BCL9	0.882	0.040	1	147579693	intron variant	C/G;T	snv			3
rs165599	ARVCF ; COMT	0.677	0.280	22	19969258	3 prime UTR variant	G/A	snv		0.56	27
rs16875288	ADAMTS16 ; LOC101929200	0.851	0.040	5	5297087	intron variant	A/T	snv		0.22	4
rs16935279	LINC01592	0.851	0.040	8	68961217	intron variant	T/C	snv		1.9E-02	4
rs17066873		0.851	0.040	13	76889874	non coding transcript exon variant	T/C	snv		5.4E-02	4
rs17154917		0.851	0.040	7	81207393	intergenic variant	G/A;T	snv			4
rs17158930	DOCK4	0.851	0.040	7	111871082	intron variant	A/G	snv		0.25	4
rs17211233	RASGRF2	0.882	0.040	5	81072944	intron variant	T/A;C	snv			4