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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
C9
(V449M)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
C9
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GBenign
C9
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
C9
(M45L)
Single nucleotide variant
(missense variant)
C9-related disorder
+2 more
GLikely benign
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