DisGeNET - a database of gene-disease associations

Source: GWASDB

Variants associated to the Disease: Protein C antigen measurement ×

Variants associated to the Gene: PROCR ×

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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
rs867186	PROCR ; MMP24-AS1-EDEM2	0.752	0.120	20	35176751	missense variant	A/G	snv	0.10	9.7E-02	5
rs2069940	MMP24-AS1-EDEM2 ; PROCR			20	35171469	upstream gene variant	C/G	snv		8.2E-02	2
rs6120870	MMP24-AS1-EDEM2 ; PROCR ; MMP24OS			20	35209685	intron variant	A/G	snv		0.19	2
rs17406518	MMP24OS ; MMP24-AS1-EDEM2 ; PROCR			20	35211373	intron variant	A/C;G	snv			2
rs6088764	MMP24OS ; MMP24-AS1-EDEM2 ; PROCR			20	35205356	intron variant	C/A	snv		0.38	2
rs11699306	MMP24OS ; PROCR ; MMP24-AS1-EDEM2			20	35213480	intron variant	T/C	snv		0.10	2
rs17092456	MMP24OS ; PROCR ; MMP24-AS1-EDEM2			20	35208389	intron variant	G/C	snv		0.13	2
rs11167260	PROCR ; MMP24-AS1-EDEM2			20	35187397	intron variant	G/A	snv		9.1E-02	2
rs6060300	PROCR ; MMP24-AS1-EDEM2			20	35193167	intron variant	T/C	snv		0.20	2
rs6087685	PROCR ; MMP24-AS1-EDEM2			20	35189809	intron variant	G/C	snv		0.40	2