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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HYDIN
(Q3133*)
Single nucleotide variant
(nonsense)
Primary ciliary dyskinesia 5
GLikely pathogenic
HYDIN
(Q2670*)
Single nucleotide variant
(nonsense)
Primary ciliary dyskinesia 5
GPathogenic
HYDIN
(R1059*)
Single nucleotide variant
(nonsense)
Primary ciliary dyskinesia 5
GPathogenic
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