DisGeNET - a database of gene-disease associations

List of shared variants

Major Depressive Disorder, C1269683

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 EXOME	AF GENOME	Num. diseases
rs2619522	DTNBP1	0.827	0.080	6	15653418	intron variant	A/C	snv		0.26	6
rs3800373	LOC101929309 ; FKBP5	0.752	0.200	6	35574699	3 prime UTR variant	C/A	snv		0.68	22
rs4713916	FKBP5	0.790	0.160	6	35702206	intron variant	A/C;G;T	snv			11
rs6937506		0.807	0.280	6	132578260	intergenic variant	G/A	snv		0.25	7
rs760761	DTNBP1	0.882	0.080	6	15650901	intron variant	G/A	snv		0.26	4
rs9296158	FKBP5 ; LOC112267956	0.763	0.080	6	35599305	intron variant	A/G	snv		0.65	16
rs9340799	ESR1	0.583	0.680	6	151842246	intron variant	A/G	snv		0.32	62
rs1045642	ABCB1	0.456	0.840	7	87509329	synonymous variant	A/G;T	snv	0.50		214
rs16139	NPY ; LOC107986777	0.658	0.560	7	24285260	missense variant	T/A;C	snv	4.0E-06; 3.0E-02		36
rs1799889	SERPINE1	0.649	0.600	7	101126430	upstream gene variant	A/G	snv			31
rs1799983	NOS3	0.430	0.880	7	150999023	missense variant	T/A;G	snv	0.75		246
rs1818879		0.827	0.120	7	22733108	downstream gene variant	G/A;C	snv			7
rs2032582	ABCB1	0.538	0.800	7	87531302	missense variant	A/C;T	snv	0.54; 3.8E-02		97
rs2070744	NOS3	0.608	0.680	7	150992991	intron variant	C/T	snv		0.70	54
rs2227631	SERPINE1	0.742	0.200	7	101126257	upstream gene variant	A/G	snv		0.54	13
rs2522833	PCLO	0.827	0.080	7	82824392	missense variant	A/C	snv	0.45	0.34	7
rs662	PON1	0.485	0.840	7	95308134	missense variant	T/C	snv	0.38	0.42	157
rs1106634	ATP6V1B2	0.851	0.080	8	20208538	intron variant	G/A;C;T	snv		0.18	5
rs4994	ADRB3	0.578	0.640	8	37966280	missense variant	A/G	snv	0.11	9.2E-02	65
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
rs1415125856	BDNF ; BDNF-AS	0.827	0.120	11	27658550	splice region variant	G/A	snv	4.0E-06	2.1E-05	7
rs1488864	LOC101927825 ; CAVIN3	0.851	0.080	11	6321099	intron variant	T/G	snv		0.80	4
rs1800497	ANKK1	0.620	0.400	11	113400106	missense variant	G/A	snv	0.26	0.26	56
rs1800532	TPH1	0.763	0.160	11	18026269	intron variant	G/T	snv		0.33	15