DisGeNET - a database of gene-disease associations

List of associated variants

Panic Disorder, C0030319

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
rs4680	COMT ; MIR4761	0.442	0.920	22	19963748	missense variant	G/A	snv	0.46	0.44	249
rs5751876	ADORA2A ; ADORA2A-AS1 ; SPECC1L-ADORA2A	0.742	0.320	22	24441333	synonymous variant	T/C	snv	0.54	0.52	16
rs10415555	PEPD	1.000	0.040	19	33519283	intron variant	A/G	snv		0.19	1
rs4804833	MAP2K7	1.000	0.040	19	7905750	intron variant	A/G;T	snv			1
rs7788	SNAPC2	1.000	0.040	19	7923232	3 prime UTR variant	T/C	snv		0.28	1
rs3813034	SLC6A4	0.827	0.160	17	30197786	3 prime UTR variant	A/C	snv		0.40	8
rs140701	SLC6A4	0.790	0.200	17	30211514	intron variant	C/T	snv		0.40	7
rs17689918	LINC02210-CRHR1 ; MAPT-AS1 ; CRHR1	0.851	0.080	17	45832722	intron variant	G/A	snv		0.15	6
rs173365	MAPT-AS1 ; LINC02210-CRHR1 ; CRHR1	0.882	0.080	17	45823708	intron variant	A/G	snv		0.55	3
rs242924	LINC02210-CRHR1 ; MAPT-AS1 ; CRHR1	0.882	0.080	17	45808001	intron variant	G/T	snv		0.44	3
rs4076452	LINC02210-CRHR1	1.000	0.040	17	45778528	intron variant	G/C	snv		0.16	2
rs3816995	SDK2	1.000	0.040	17	73339121	intron variant	G/A	snv		0.40	1
rs4583306	SLC6A4	1.000	0.040	17	30211697	intron variant	A/G	snv		0.37	1
rs4795942	TMEM132E	1.000	0.040	17	34584149	intron variant	C/T	snv		0.72	1
rs6502892	MIR22 ; MIR22HG	1.000	0.040	17	1714314	intron variant	T/C;G	snv			1
rs8076112	TLCD2	1.000	0.040	17	1708905	intron variant	A/C;G	snv		0.15	1
rs887230	C17orf102	1.000	0.040	17	34577567	non coding transcript exon variant	C/T	snv	0.82	0.85	1
rs887231	C17orf102	1.000	0.040	17	34577461	non coding transcript exon variant	G/A	snv		0.73	1
rs2242446	SLC6A2	0.776	0.080	16	55656513	5 prime UTR variant	C/A;T	snv			9
rs1805067	SLC6A2	0.925	0.080	16	55698511	missense variant	G/A	snv	2.8E-05	2.1E-05	2
rs945032	BDKRB2	0.882	0.040	14	96204324	upstream gene variant	T/C	snv		0.78	5
rs6313	HTR2A	0.562	0.640	13	46895805	synonymous variant	G/A	snv	0.41	0.40	82
rs75634836	HTR2A	0.807	0.160	13	46835532	missense variant	C/A;T	snv	4.0E-06		11
rs1326656542	LIG4	0.776	0.280	13	108210293	missense variant	A/T	snv	4.0E-06		10
rs2296972	HTR2A-AS1 ; HTR2A	0.925	0.080	13	46854336	intron variant	A/C	snv		0.70	4