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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
C3
(G1623W)
Single nucleotide variant
(missense variant)
not provided
+3 more
GUncertain significance
C3
(S1619R)
Single nucleotide variant
(missense variant)
Complement component 3 deficiency
+4 more
GConflicting classifications of pathogenicity
C3
(D1115N)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
C3
(K65Q)
Single nucleotide variant
(missense variant)
Complement component 3 deficiency
+4 more
GConflicting classifications of pathogenicity
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