DisGeNET - a database of gene-disease associations

Source: ALL

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

Variants associated to the Gene: FAM222B ×

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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
rs9892942	FAM222B			17	28851743	intron variant	C/T	snv		0.25	4
rs7215310	FAM222B			17	28761608	intron variant	C/A	snv		0.19	2
rs11650788	FAM222B			17	28847505	intron variant	T/A	snv		0.25	1