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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC108281160, MASP1
(G35C)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LOC108281160, MASP1
(W3R)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance