DisGeNET - a database of gene-disease associations

Source: ALL

Results per page

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
rs9939609	FTO	0.559	0.720	16	53786615	intron variant	T/A	snv	0.41	98
rs8050136	FTO	0.716	0.560	16	53782363	intron variant	C/A	snv	0.40	32
rs10830963	MTNR1B	0.776	0.400	11	92975544	intron variant	C/G	snv	0.22	27
rs657152	ABO	0.882	0.200	9	133263862	intron variant	A/C;T	snv		22
rs1121980	FTO	0.807	0.240	16	53775335	intron variant	G/A;C	snv		18
rs9930506	FTO	0.776	0.360	16	53796553	intron variant	A/G	snv	0.36	16
rs687289	ABO	1.000	0.120	9	133261703	intron variant	A/G	snv		15
rs965513	PTCSC2	0.742	0.200	9	97793827	intron variant	A/G;T	snv		15
rs9940128	FTO	0.851	0.120	16	53766842	intron variant	G/A	snv	0.42	10
rs1443438	PTCSC2	0.827	0.080	9	97787746	intron variant	T/A;C	snv		8
rs507666	ABO	1.000	0.040	9	133273983	intron variant	A/G	snv		8
rs7193144	FTO	0.925	0.120	16	53776774	intron variant	T/C	snv	0.40	6
rs7850258	PTCSC2	0.827	0.200	9	97786731	intron variant	A/G	snv	0.72	6
rs925489	PTCSC2	0.882	0.080	9	97784318	intron variant	C/T	snv	0.71	6
rs3741298	ZPR1			11	116786845	intron variant	C/T	snv	0.73	5
rs9926289	FTO	0.882	0.160	16	53786591	intron variant	G/A	snv	0.41	5
rs10759944	PTCSC2	0.925	0.080	9	97794690	intron variant	A/G	snv	0.72	4
rs13077101	RABL3			3	120706484	intron variant	T/C	snv		4
rs1912826	KLKB1			4	186228386	intron variant	G/A;C	snv		4
rs2078087	NMNAT2			1	183389270	intron variant	C/T	snv	0.16	4
rs4253238	KLKB1	0.925	0.080	4	186227233	intron variant	C/T	snv	0.59	4
rs7028661	PTCSC2	0.882	0.080	9	97776188	intron variant	A/G	snv	0.72	4
rs7726839	CEP72			5	618471	intron variant	A/G	snv	0.31	4
rs892295	CHL1			3	355870	intron variant	A/G	snv	0.87	4
rs9939973	FTO	1.000	0.080	16	53766656	intron variant	G/A	snv	0.42	4