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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NME8
Single nucleotide variant
(intron variant)
Primary ciliary dyskinesia
+3 more
GBenign/Likely benign
NME8
(L426*)
Single nucleotide variant
(nonsense)
Primary ciliary dyskinesia
+1 more
GUncertain significance