DisGeNET - a database of gene-disease associations

Source: GWASDB ×

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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
rs1121980	FTO	0.807	0.240	16	53775335	intron variant	G/A;C	snv			9
rs7903146	TCF7L2	0.554	0.680	10	112998590	intron variant	C/G;T	snv			8
rs7138803		0.827	0.240	12	49853685	intergenic variant	G/A;T	snv			6
rs17817449	FTO	0.716	0.560	16	53779455	intron variant	T/A;G	snv			5
rs7498665	SH2B1	0.925	0.120	16	28871920	missense variant	A/G;T	snv	0.35		5
rs11075989	FTO	0.925	0.120	16	53785965	intron variant	C/A;T	snv			3
rs11642841	FTO	0.925	0.120	16	53811575	intron variant	C/A;G	snv			3
rs7185735	FTO	0.925	0.120	16	53788739	intron variant	A/G;T	snv			3
rs8044769	FTO	0.851	0.200	16	53805223	intron variant	T/A;C;G	snv			3
rs10852521	FTO	1.000	0.080	16	53771053	intron variant	T/A;C	snv			2
rs11152213		1.000	0.080	18	60185715	intergenic variant	A/C;T	snv			2
rs12446228	FTO	1.000	0.080	16	53766475	intron variant	A/G;T	snv			2
rs17817288	FTO	1.000	0.080	16	53773852	intron variant	A/C;G	snv			2
rs9923233	FTO	1.000	0.080	16	53785286	intron variant	G/A;C	snv			2
rs9930333	FTO	0.882	0.120	16	53766065	intron variant	T/C;G	snv			2
rs127430	APCDD1L-DT			20	58589799	intron variant	A/G;T	snv			1
rs1440072	KCNE4			2	223072020	intron variant	C/A;G;T	snv			1
rs489693		1.000	0.080	18	60215554	intergenic variant	C/A;T	snv			1
rs7601155	BABAM2			2	28124815	intron variant	C/T	snv		6.8E-02	1
rs7890572	IL1RAPL1			X	29622701	intron variant	A/G	snv		9.3E-02	1
rs12446632	LOC105371116	1.000	0.080	16	19924067	intergenic variant	G/A	snv		0.11	1
rs2075650	TOMM40	0.662	0.360	19	44892362	intron variant	A/G	snv	0.13	0.13	20
rs11847697	PRKD1			14	30045906	intron variant	C/T	snv		0.13	2
rs2287019	QPCTL	1.000	0.080	19	45698914	intron variant	C/T	snv	0.17	0.16	2
rs633715		1.000	0.080	1	177883445	intron variant	T/C	snv		0.17	4