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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CCDC39, TTC14
(S888fs)
Duplication
(frameshift variant +1 more)
not provided
+2 more
GBenign/Likely benign
CCDC39, TTC14
(I845T)
Single nucleotide variant
(missense variant +1 more)
not specified
+3 more
GConflicting classifications of pathogenicity