DisGeNET - a database of gene-disease associations

List of associated variants

Obesity, C0028754

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 GENOME	Num. diseases
rs999943	ITPR3	1.000	0.080	6	33656956	intron variant	A/G	snv	0.28	1
rs9986517	CPNE5	1.000	0.080	6	36751302	intron variant	C/A;T	snv		1
rs997509	ENPP1	0.827	0.200	6	131846837	intron variant	C/T	snv	5.3E-02	6
rs9956279		1.000	0.080	18	60275566	intergenic variant	C/A;T	snv		1
rs9947301		1.000	0.080	18	60202357	downstream gene variant	C/T	snv	9.7E-02	1
rs9941349	FTO	1.000	0.080	16	53791576	intron variant	C/T	snv	0.34	6
rs9940646	FTO	1.000	0.080	16	53766717	intron variant	C/G	snv	0.42	2
rs9940128	FTO	0.851	0.120	16	53766842	intron variant	G/A	snv	0.42	10
rs9939973	FTO	1.000	0.080	16	53766656	intron variant	G/A	snv	0.42	4
rs9939609	FTO	0.559	0.720	16	53786615	intron variant	T/A	snv	0.41	98
rs9939506	TOX3	1.000	0.080	16	52494395	intron variant	T/C;G	snv		1
rs9937053	FTO	0.882	0.160	16	53765595	intron variant	G/A	snv	0.42	6
rs9936385	FTO	0.925	0.120	16	53785257	intron variant	T/C	snv	0.41	5
rs9935401	FTO	0.925	0.120	16	53782926	intron variant	G/A	snv	0.40	3
rs9932754	FTO	1.000	0.080	16	53796579	intron variant	T/C	snv	0.36	2
rs9931494	FTO	1.000	0.080	16	53793267	intron variant	C/G	snv	0.34	2
rs9930506	FTO	0.776	0.360	16	53796553	intron variant	A/G	snv	0.36	16
rs9930501	FTO	1.000	0.080	16	53796540	intron variant	A/G	snv	0.36	2
rs9930333	FTO	0.882	0.120	16	53766065	intron variant	T/C;G	snv		7
rs9928094	FTO	1.000	0.080	16	53765993	intron variant	A/G	snv	0.42	3
rs9923544	FTO	1.000	0.080	16	53768073	intron variant	C/T	snv	0.42	3
rs9923451	WWOX	1.000	0.080	16	78918542	intron variant	A/C;G	snv		1
rs9923233	FTO	1.000	0.080	16	53785286	intron variant	G/A;C	snv		2
rs9923147	FTO	1.000	0.080	16	53767637	intron variant	C/T	snv	0.42	2
rs9922708	FTO	1.000	0.080	16	53797234	intron variant	C/T	snv	0.36	2