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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FCN3
(R255H +1 more)
Single nucleotide variant
(missense variant)
Immunodeficiency due to ficolin3 deficiency
GUncertain significance
FCN3
(W136L +1 more)
Single nucleotide variant
(missense variant)
Immunodeficiency due to ficolin3 deficiency
GUncertain significance