Related gene-specific medical variations for Gene (Select 8547) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2441403	NM_003665.4(FCN3):c.440G>T (p.Trp147Leu)	FCN3 (W136L +1 more)	Single nucleotide variant (missense variant)	Immunodeficiency due to ficolin3 deficiency	GUncertain significance
Select item 2441402	NM_003665.4(FCN3):c.797G>A (p.Arg266His)	FCN3 (R255H +1 more)	Single nucleotide variant (missense variant)	Immunodeficiency due to ficolin3 deficiency	GUncertain significance