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 EXOME	AF GENOME	Num. diseases
rs4129267	IL6R	0.807	0.200	1	154453788	intron variant	C/G;T	snv			13
rs7310615	SH2B3	0.882		12	111427245	intron variant	C/G	snv		0.67	12
rs4537545	IL6R	0.790	0.160	1	154446403	intron variant	C/T	snv		0.48	11
rs12239046	NLRP3			1	247438293	intron variant	T/C	snv		0.58	9
rs10519203	HYKK	0.851	0.080	15	78521704	intron variant	G/A	snv		0.67	8
rs7529229	IL6R	0.851	0.120	1	154448302	intron variant	T/C	snv		0.48	8
rs1539019	NLRP3	0.882	0.240	1	247436999	intron variant	A/C	snv		0.63	6
rs3091307	TH2LCRR	0.925	0.160	5	132653444	intron variant	A/G	snv		0.34	6
rs2066861	FGG			4	154606284	intron variant	C/T	snv		0.26	5
rs2158177	TH2LCRR	0.925	0.120	5	132648366	intron variant	A/G	snv		0.18	5
rs10512597	RAB37 ; CD300LF			17	74703694	intron variant	T/A;C	snv			4
rs2070016	FGA	1.000	0.040	4	154589162	intron variant	A/G	snv		0.12	4
rs2073643	SLC22A5	1.000	0.080	5	132387596	intron variant	T/C	snv		0.46	4
rs2522056	IRF1-AS1			5	132466034	intron variant	G/A	snv		0.25	4
rs61812598	IL6R	1.000	0.080	1	154447611	intron variant	G/A	snv		0.31	4
rs7518199	IL6R			1	154434943	intron variant	A/C;T	snv	0.39; 4.2E-06		4
rs10157379	NLRP3			1	247442297	intron variant	C/G;T	snv			3
rs10489615	GALNT2			1	230169242	intron variant	A/C;G	snv			3
rs11242111	LINC02863 ; IRF1-AS1			5	132420366	intron variant	A/G;T	snv			3
rs12651106	DCHS2			4	154379907	intron variant	C/A	snv		0.12	3
rs12712127	IL1R1			2	102110201	intron variant	A/G	snv		0.62	3
rs12915708	SPPL2A			15	50756405	intron variant	G/A;C	snv			3
rs1476698	FARP2			2	241357034	intron variant	A/G;T	snv			3
rs17690122				5	132532143	intron variant	A/G;T	snv			3
rs2106854	IRF1-AS1			5	132433482	intron variant	C/T	snv		0.23	3