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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
STK36
(L840V)
Single nucleotide variant
(missense variant +1 more)
Ciliary dyskinesia, primary, 46
+1 more
GBenign/Likely benign
STK36
Single nucleotide variant
(synonymous variant)
Ciliary dyskinesia, primary, 46
+1 more
GBenign