DisGeNET - a database of gene-disease associations

Source: GWASCAT

Variants associated to the Disease: C-reactive protein measurement ×

Variants associated to the Gene: GCKR ×

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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
rs1260326	GCKR	0.645	0.600	2	27508073	missense variant	T/C;G	snv	0.63; 4.0E-06	0.68	55
rs780094	GCKR	0.658	0.400	2	27518370	intron variant	T/C	snv		0.67	35
rs780093	GCKR	0.763	0.240	2	27519736	intron variant	T/C	snv		0.68	16
rs3817588	GCKR	0.882	0.160	2	27508345	intron variant	T/C	snv		0.14	3
rs814295	GCKR	0.925	0.120	2	27520348	intron variant	A/G	snv		0.18	2