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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CCDC39, TTC14
(T872K)
Single nucleotide variant
(missense variant +1 more)
not provided
+2 more
GUncertain significance
CCDC39, TTC14
(R829C)
Single nucleotide variant
(missense variant +1 more)
Primary ciliary dyskinesia
+2 more
GUncertain significance