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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
C1D
(V133G)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
C1D
(W68L)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance