DisGeNET - a database of gene-disease associations

List of associated variants

Mood Disorders, C0525045

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
rs1805054	HTR6	0.708	0.200	1	19666020	synonymous variant	C/T	snv	0.15; 8.0E-06	0.16	17
rs659366	UCP2	0.724	0.520	11	73983709	non coding transcript exon variant	C/T	snv		0.40	17
rs2230912	P2RX7 ; LOC105370032	0.752	0.280	12	121184393	missense variant	A/G	snv	0.13	0.12	16
rs1800532	TPH1	0.763	0.160	11	18026269	intron variant	G/T	snv		0.33	15
rs2251219	SMIM4 ; PBRM1	0.732	0.120	3	52550771	synonymous variant	T/C;G	snv	0.39; 4.0E-06	0.34	14
rs135745		0.763	0.200	22	38287631	downstream gene variant	G/C	snv		0.48	13
rs1289543302	ABCB1	0.763	0.440	7	87536472	missense variant	C/T	snv			12
rs10994336	ANK3	0.776	0.160	10	60420054	intron variant	C/T	snv		7.5E-02	12
rs12273363	BDNF	0.807	0.120	11	27723312	intron variant	T/C	snv		0.16	11
rs4713916	FKBP5	0.790	0.160	6	35702206	intron variant	A/C;G;T	snv			11
rs7997012	HTR2A	0.807	0.080	13	46837850	intron variant	A/G	snv		0.69	11
rs734312	WFS1	0.790	0.240	4	6301627	missense variant	G/A	snv	0.55	0.42	10
rs779867	GRM7	0.776	0.120	3	7442784	intron variant	T/C;G	snv			9
rs2271933	HCRTR1	0.807	0.080	1	31626924	missense variant	A/G	snv	0.56	0.50	9
rs208294	P2RX7 ; LOC105370032	0.790	0.320	12	121162450	missense variant	T/A;C;G	snv	0.51		9
rs28364997	SLC6A3	0.807	0.120	5	1403013	missense variant	G/A	snv	5.3E-04	5.8E-04	9
rs3771829	TACR1	0.790	0.120	2	75137019	intron variant	C/G	snv		0.11	9
rs841	GCH1	0.827	0.200	14	54843774	splice region variant	G/A	snv	0.22	0.22	8
rs10748842	NRG3	0.807	0.120	10	81889983	intron variant	T/C	snv		0.13	8
rs908867		0.851	0.160	11	27724217	intron variant	C/G;T	snv			7
rs6675281	DISC2 ; DISC1 ; TSNAX-DISC1 ; LOC105373170	0.827	0.080	1	231818355	missense variant	C/T	snv	0.11	0.14	7
rs9370822	DTNBP1 ; LOC105374947	0.882	0.120	6	15544505	intron variant	A/C	snv		0.36	7
rs2072621	GPR50-AS1 ; GPR50	0.851	0.080	X	151177387	non coding transcript exon variant	C/A;G	snv			7
rs6782011	GRM7	0.807	0.120	3	7457960	intron variant	C/T	snv		0.52	7
rs7225002	KANSL1	0.925	0.080	17	46111701	intron variant	A/G	snv		0.39	7