DisGeNET - a database of gene-disease associations

Source: GWASCAT

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

Variants associated to the Gene: CCDC162P ×

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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
rs9487023	CCDC162P			6	109268801	intron variant	A/G	snv		0.40	8
rs200980971	CCDC162P			6	109261139	intron variant	A/-;AA	delins			2
rs36052053	CCDC162P			6	109262596	intron variant	G/A	snv		0.11	2
rs6568570	CCDC162P			6	109292038	intron variant	T/A;C;G	snv			2
rs9480924	CCDC162P			6	109295867	intron variant	T/C	snv		0.40	2