DisGeNET - a database of gene-disease associations

Source: GWASCAT

Variants associated to the Disease: Red cell distribution width determination ×

Variants associated to the Gene: C18orf25 ×

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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
rs3842397	C18orf25			18	46265918	3 prime UTR variant	TT/-	del		0.43	3
rs9944715	C18orf25			18	46251293	intron variant	A/G	snv		0.62	3
rs12963943	C18orf25			18	46225695	intron variant	C/T	snv		0.61	2
rs144667737	C18orf25			18	46189157	intron variant	G/A	snv		1.1E-02	2