DisGeNET - a database of gene-disease associations

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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
rs75885714	PLCL2			3	16901018	intron variant	A/C	snv		4.6E-02	7
rs116577908	PLCL2			3	17056907	intron variant	A/G	snv		7.1E-03	4
rs73146904	PLCL2			3	16891490	intron variant	G/A	snv		9.4E-02	3
rs1372072	PLCL2	0.851	0.200	3	16913767	intron variant	G/A	snv		0.35	2
rs9846711	PLCL2	1.000	0.040	3	16821370	intron variant	T/C	snv		0.58	2
rs4685408	PLCL2	0.925	0.040	3	16954543	intron variant	G/A	snv		0.56	2
rs7613595	PLCL2			3	16867007	intron variant	C/A	snv		0.79	2
rs7653834	PLCL2	0.925	0.040	3	17009836	synonymous variant	T/C	snv	0.37	0.38	2
rs114893614	PLCL2			3	16891211	intron variant	C/T	snv		4.1E-02	2
rs9821630	PLCL2			3	16929446	intron variant	A/G	snv		0.24	2
rs6804663	PLCL2	1.000	0.040	3	16833950	intron variant	G/A	snv		0.58	2
rs9858071	PLCL2	1.000	0.040	3	16803898	intron variant	T/C	snv		0.37	2
rs2278609	PLCL2 ; LOC105376972	1.000	0.040	3	16882947	intron variant	C/A;G;T	snv			2
rs1992381	LOC105376972 ; PLCL2			3	16886567	intron variant	T/A;C	snv			1
rs143759545	LOC105376972 ; PLCL2			3	16884567	intron variant	C/G;T	snv			1
rs4452313	PLCL2	1.000	0.120	3	17005540	intron variant	A/T	snv		0.40	1
rs144614991	PLCL2			3	16925189	intron variant	C/T	snv		3.9E-02	1
rs748832	PLCL2			3	16809700	intron variant	G/A	snv		0.59	1
rs73139274	PLCL2			3	16817019	intron variant	C/G	snv		0.16	1
rs6779302	PLCL2			3	16818207	intron variant	T/A;G	snv			1
rs73139272	PLCL2			3	16816965	intron variant	G/A;T	snv			1
rs4618210	PLCL2	1.000	0.080	3	17082892	intron variant	A/G	snv		0.56	1
rs9852648	PLCL2			3	16869827	intron variant	G/A	snv		0.76	1
rs79638618	PLCL2			3	16890061	intron variant	C/T	snv		3.7E-02	1
rs200726463	PLCL2			3	16992491	intron variant	-/AG	delins		7.1E-03	1