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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CCDC65
(N62D)
Single nucleotide variant
(5 prime UTR variant +1 more)
Primary ciliary dyskinesia 27
GUncertain significance
CCDC65
Single nucleotide variant
(intron variant)
Primary ciliary dyskinesia 27
GUncertain significance
CCDC65
(D427G +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
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