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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ODAD3
Single nucleotide variant
(splice donor variant)
Primary ciliary dyskinesia 30
GUncertain significance
ODAD3
(K305R +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+2 more
GUncertain significance
ODAD3
(S132G +2 more)
Single nucleotide variant
(missense variant)
Primary ciliary dyskinesia 30
GUncertain significance
ODAD3
(Y141* +1 more)
Single nucleotide variant
(nonsense +1 more)
Primary ciliary dyskinesia 30
GLikely pathogenic
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