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
rs495225	GHSR	0.882	0.040	3	172448243	synonymous variant	G/A;C;T	snv	0.66		4
rs4148087	ABCG1	1.000	0.040	21	42202157	intron variant	G/A;T	snv			3
rs41423247	NR3C1	0.695	0.440	5	143399010	intron variant	G/C	snv		0.31	23
rs9939609	FTO	0.559	0.720	16	53786615	intron variant	T/A	snv		0.41	98
rs4869317	LNPEP	1.000	0.040	5	96956300	intron variant	T/A	snv		0.22	2
rs56149945	NR3C1	0.595	0.680	5	143399752	missense variant	T/A;C	snv	2.0E-02		49
rs16139	NPY ; LOC107986777	0.658	0.560	7	24285260	missense variant	T/A;C	snv	4.0E-06; 3.0E-02		36
rs3798577	ESR1	0.742	0.320	6	152099995	3 prime UTR variant	T/C	snv		0.45	16
rs6198	NR3C1	0.724	0.480	5	143278056	3 prime UTR variant	T/C	snv		0.12	16
rs375382379	NR3C1	0.882	0.160	5	143399792	missense variant	T/C	snv	4.0E-06		5
rs550659379	NR3C1	0.882	0.160	5	143399780	missense variant	T/C	snv	4.0E-06	7.0E-06	5
rs752834812	NR3C1	0.882	0.160	5	143399885	missense variant	T/C	snv	8.0E-06		5
rs7180942	NTRK3			15	88131345	intron variant	T/C	snv		0.56	1
rs2501432	CNR2	0.716	0.480	1	23875430	missense variant	T/C;G	snv	0.62		16
rs13438494	PCLO	1.000	0.040	7	82759398	intron variant	T/G	snv		0.61	6
rs879761216	CNR2	0.732	0.480	1	23875429	frameshift variant	TT/C;T	delins			14
rs35761398	CNR2	0.701	0.520	1	23875429	missense variant	TT/CC	mnv			19