DisGeNET - a database of gene-disease associations

List of associated variants

Agoraphobia, C0001818

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
rs6295	HTR1A	0.645	0.200	5	63962738	intron variant	C/G	snv		0.49	40
rs1718119	LOC105370032 ; P2RX7	0.689	0.520	12	121177300	missense variant	G/A;T	snv	0.35; 4.0E-06		21
rs324981	NPSR1-AS1 ; NPSR1	0.724	0.320	7	34778501	missense variant	A/T	snv	0.44	0.47	18
rs5751876	ADORA2A ; ADORA2A-AS1 ; SPECC1L-ADORA2A	0.742	0.320	22	24441333	synonymous variant	T/C	snv	0.54	0.52	16
rs2271933	HCRTR1	0.807	0.080	1	31626924	missense variant	A/G	snv	0.56	0.50	9
rs3817190	CAMKK2	0.851	0.080	12	121274274	missense variant	T/A;G	snv	0.38		6
rs7688285		0.925	0.040	4	157047466	intergenic variant	G/A	snv		0.10	2
rs17035816	GLRB	0.925	0.040	4	157167312	intron variant	A/G	snv		0.11	2
rs11946004	NPY5R	0.925	0.040	4	163351551	synonymous variant	G/A;T	snv	0.10; 4.0E-06		2
rs11724320	NPY5R ; NPY1R	0.925	0.040	4	163346771	intron variant	T/C	snv		0.56	2
rs17303244	RORA	1.000	0.040	15	60908101	intron variant	T/C	snv		0.12	1