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
rs814295	GCKR	0.925	0.120	2	27520348	intron variant	A/G	snv		0.18	5
rs9268858	HLA-DRB9	0.882	0.200	6	32461981	intron variant	T/C	snv		0.29	5
rs1169313	C12orf43			12	121004867	intron variant	T/A;C	snv			4
rs12239046	NLRP3			1	247438293	intron variant	T/C	snv		0.58	4
rs13233571	BCL7B	0.925	0.120	7	73556901	intron variant	C/T	snv		9.2E-02	4
rs1558902	FTO	0.827	0.120	16	53769662	intron variant	T/A	snv		0.31	4
rs2244608	HNF1A ; HNF1A-AS1	0.882	0.160	12	120979185	intron variant	A/G	snv		0.29	4
rs3758348	SURF4			9	133372523	intron variant	G/C	snv		0.13	4
rs4537545	IL6R	0.790	0.160	1	154446403	intron variant	C/T	snv		0.48	4
rs7518199	IL6R			1	154434943	intron variant	A/C;T	snv	0.39; 4.2E-06		4
rs7529229	IL6R	0.851	0.120	1	154448302	intron variant	T/C	snv		0.48	4
rs10512597	RAB37 ; CD300LF			17	74703694	intron variant	T/A;C	snv			3
rs13244268	BAZ1B	0.925	0.120	7	73497513	intron variant	T/C	snv		9.2E-02	3
rs157582	TOMM40	0.851	0.160	19	44892962	intron variant	C/T	snv	0.24	0.29	3
rs2393791	HNF1A	0.925	0.160	12	120986153	intron variant	C/T	snv		0.62	3
rs3817588	GCKR	0.882	0.160	2	27508345	intron variant	T/C	snv		0.14	3
rs4845625	IL6R	0.851	0.080	1	154449591	intron variant	T/C	snv		0.60	3
rs7310409	HNF1A	0.925	0.160	12	120987058	intron variant	A/C;G;T	snv			3
rs10518765	UNC13C	1.000	0.040	15	54388434	intron variant	A/C	snv		0.16	2
rs10761731	JMJD1C			10	63267850	intron variant	A/T	snv		0.38	2
rs10891343	BCO2			11	112209661	intron variant	T/C	snv		0.44	2
rs10908713				1	159369769	intron variant	T/C	snv		0.47	2
rs11265174				1	159350569	intron variant	T/A	snv		0.35	2
rs11265190	OR10J1			1	159421611	intron variant	G/A	snv		0.47	2
rs11265196				1	159448422	intron variant	G/A	snv		0.47	2