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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
C9
(D454N)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
C9
(R271Q)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
C9
Single nucleotide variant
not provided
GLikely benign
C9
(M45L)
Single nucleotide variant
(missense variant)
not provided
+2 more
GLikely benign
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