DisGeNET - a database of gene-disease associations

List of associated variants

Eating Disorders, C0013473

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
rs13077017	FLNB			3	58120049	intron variant	C/T	snv		0.21	2
rs13086738	SOX2-OT	1.000	0.040	3	181080939	intron variant	A/G	snv		0.21	3
rs4869317	LNPEP	1.000	0.040	5	96956300	intron variant	T/A	snv		0.22	2
rs1805576	FXR1	1.000	0.040	3	180949777	intron variant	C/G;T	snv		0.24	3
rs1800497	ANKK1	0.620	0.400	11	113400106	missense variant	G/A	snv	0.26	0.26	56
rs41423247	NR3C1	0.695	0.440	5	143399010	intron variant	G/C	snv		0.31	23
rs6313	HTR2A	0.562	0.640	13	46895805	synonymous variant	G/A	snv	0.41	0.40	82
rs6311	HTR2A	0.645	0.640	13	46897343	upstream gene variant	C/T	snv		0.40	41
rs9939609	FTO	0.559	0.720	16	53786615	intron variant	T/A	snv		0.41	98
rs4680	COMT ; MIR4761	0.442	0.920	22	19963748	missense variant	G/A	snv	0.46	0.44	249
rs3798577	ESR1	0.742	0.320	6	152099995	3 prime UTR variant	T/C	snv		0.45	16
rs12475512				2	231433365	downstream gene variant	G/A	snv		0.47	2
rs7180942	NTRK3			15	88131345	intron variant	T/C	snv		0.56	1
rs13438494	PCLO	1.000	0.040	7	82759398	intron variant	T/G	snv		0.61	6
rs10858583	LOC107984478	1.000	0.040	12	87334666	intergenic variant	C/T	snv		0.79	3
rs1473473	TPH2	0.925	0.080	12	72010598	intron variant	C/A;T	snv		0.81	4
rs5522	NR3C2	0.732	0.320	4	148436323	missense variant	C/T	snv	0.88	0.89	19