DisGeNET - a database of gene-disease associations

List of shared variants

Complement Factor I (C3 inactivator) deficiency, C3463916

Disease: Congenital hypofibrinogenemia

Source: ALL

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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
rs121909621	FGB	0.925	0.120	4	154569703	missense variant	T/G	snv			2
rs121909622	FGB	0.925	0.120	4	154570463	missense variant	G/A	snv			2