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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TP73
(V377M +2 more)
Single nucleotide variant
(missense variant +1 more)
Ciliary dyskinesia, primary, 47, and lissencephaly
GUncertain significance
TP73
(R393C +6 more)
Single nucleotide variant
(missense variant +1 more)
Ciliary dyskinesia, primary, 47, and lissencephaly
GUncertain significance