DisGeNET - a database of gene-disease associations

List of shared variants

Major Depressive Disorder, C1269683

Disease: Depressive Symptoms

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
rs2227631	SERPINE1	0.742	0.200	7	101126257	upstream gene variant	A/G	snv		0.54	13
rs1799889	SERPINE1	0.649	0.600	7	101126430	upstream gene variant	A/G	snv			31
rs161645	LOC105379109	1.000	0.040	5	104734216	intron variant	A/G	snv		0.77	2
rs2287161	MTERF2	0.827	0.080	12	106987362	upstream gene variant	C/G;T	snv			7
rs1143634	IL1B	0.597	0.680	2	112832813	synonymous variant	G/A	snv	0.19	0.19	52
rs16944	IL1B	0.531	0.920	2	112837290	upstream gene variant	A/G	snv		0.57	92
rs1800497	ANKK1	0.620	0.400	11	113400106	missense variant	G/A	snv	0.26	0.26	56
rs7973260	KSR2	0.851	0.120	12	117937681	intron variant	A/G	snv		0.83	7
rs1217691063	MTHFR	0.330	0.920	1	11796309	missense variant	A/G	snv	4.0E-06	7.0E-06	614
rs1200746244	MTHFR	0.807	0.080	1	11801287	missense variant	C/T	snv	4.0E-06	7.0E-06	11
rs2230912	P2RX7 ; LOC105370032	0.752	0.280	12	121184393	missense variant	A/G	snv	0.13	0.12	16
rs6198	NR3C1	0.724	0.480	5	143278056	3 prime UTR variant	T/C	snv		0.12	16
rs6191	NR3C1	0.925	0.040	5	143278591	3 prime UTR variant	C/A	snv		0.48	4
rs33388	NR3C1	0.776	0.360	5	143317730	intron variant	A/T	snv		0.53	12
rs41423247	NR3C1	0.695	0.440	5	143399010	intron variant	G/C	snv		0.31	23
rs5522	NR3C2	0.732	0.320	4	148436323	missense variant	C/T	snv	0.88	0.89	19
rs2234693	ESR1	0.555	0.680	6	151842200	intron variant	T/C	snv		0.47	77
rs9340799	ESR1	0.583	0.680	6	151842246	intron variant	A/G	snv		0.32	62
rs4680	COMT ; MIR4761	0.442	0.920	22	19963748	missense variant	G/A	snv	0.46	0.44	249
rs749437638	ARVCF ; COMT	0.752	0.240	22	19968597	missense variant	C/T	snv	2.4E-05	1.4E-05	14
rs165599	ARVCF ; COMT	0.677	0.280	22	19969258	3 prime UTR variant	G/A	snv		0.56	27
rs7124442	BDNF-AS ; BDNF	0.827	0.160	11	27655494	3 prime UTR variant	C/G;T	snv			9
rs6265	BDNF ; BDNF-AS	0.436	0.760	11	27658369	missense variant	C/T	snv	0.19	0.15	272
rs759834365	BDNF-AS ; BDNF	0.448	0.760	11	27658456	missense variant	C/T	snv	1.2E-05		237
rs25531	SLC6A4 ; LOC105371720	0.581	0.520	17	30237328	upstream gene variant	T/C	snv		0.18	72