DisGeNET - a database of gene-disease associations

Source: GWASCAT

Variants associated to the Disease: Finding of Mean Corpuscular Hemoglobin ×

Variants associated to the Gene: PLCL2 ×

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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
rs115792481	PLCL2			3	16898659	intron variant	G/T	snv		4.6E-02	1
rs116577908	PLCL2			3	17056907	intron variant	A/G	snv		7.1E-03	4
rs143759545	LOC105376972 ; PLCL2			3	16884567	intron variant	C/G;T	snv			1
rs2060597	PLCL2			3	16847490	intron variant	T/C	snv		3.5E-02	1
rs73146904	PLCL2			3	16891490	intron variant	G/A	snv		9.4E-02	3
rs9821630	PLCL2			3	16929446	intron variant	A/G	snv		0.24	2