DisGeNET - a database of gene-disease associations

List of shared variants

Unipolar Depression, C0041696

Disease: Depressive 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 GENOME	Num. diseases
rs1006737	CACNA1C	0.695	0.120	12	2236129	intron variant	G/A	snv	0.36	27
rs10514299	TMEM161B-AS1	0.827	0.120	5	88367793	intron variant	C/T	snv	0.21	6
rs11030101	BDNF-AS ; BDNF	0.763	0.160	11	27659197	5 prime UTR variant	A/T	snv	0.36	10
rs11904814	CREB1	0.851	0.080	2	207562074	intron variant	T/G	snv	0.30	5
rs1360780	FKBP5 ; LOC112267956	0.708	0.320	6	35639794	intron variant	T/A;C	snv		31
rs1432441	MAP2K1	0.882	0.040	15	66426943	intron variant	G/A	snv	0.27	3
rs1488864	LOC101927825 ; CAVIN3	0.851	0.080	11	6321099	intron variant	T/G	snv	0.80	4
rs1545843	LOC107984536	0.827	0.120	12	84170289	intron variant	G/A	snv	0.52	6
rs1549854	MAP2K1	0.882	0.040	15	66404397	intron variant	A/C;G	snv	0.44	3
rs174697	ARVCF ; COMT	0.851	0.080	22	19966309	intron variant	A/G	snv	0.88	5
rs1799752	ACE	0.677	0.480	17	63488529	intron variant	-/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT	delins		25
rs1800532	TPH1	0.763	0.160	11	18026269	intron variant	G/T	snv	0.33	15
rs1800587	IL1A	0.620	0.720	2	112785383	upstream gene variant	G/A;C	snv	0.32	43
rs2234693	ESR1	0.555	0.680	6	151842200	intron variant	T/C	snv	0.47	77
rs2242446	SLC6A2	0.776	0.080	16	55656513	5 prime UTR variant	C/A;T	snv		9
rs2253206		0.851	0.080	2	207527254	intron variant	A/G	snv	0.47	6
rs25531	SLC6A4 ; LOC105371720	0.581	0.520	17	30237328	upstream gene variant	T/C	snv	0.18	72
rs334558	LOC107986119 ; GSK3B	0.701	0.320	3	120094435	upstream gene variant	A/G	snv	0.51	20
rs397507444	MTHFR	0.405	0.880	1	11794407	missense variant	T/G	snv		306
rs41423247	NR3C1	0.695	0.440	5	143399010	intron variant	G/C	snv	0.31	23
rs4713916	FKBP5	0.790	0.160	6	35702206	intron variant	A/C;G;T	snv		11
rs53576	OXTR ; CAV3	0.641	0.320	3	8762685	intron variant	A/G;T	snv		42
rs61888800	BDNF	0.851	0.080	11	27700731	5 prime UTR variant	G/T	snv	0.19	5
rs6295	HTR1A	0.645	0.200	5	63962738	intron variant	C/G	snv	0.49	40
rs6311	HTR2A	0.645	0.640	13	46897343	upstream gene variant	C/T	snv	0.40	41