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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CEP120
(K348* +3 more)
Single nucleotide variant
(nonsense +1 more)
Short-rib thoracic dysplasia 13 with or without polydactyly
+1 more
GPathogenic/Likely pathogenic
CEP120
(A199P +2 more)
Single nucleotide variant
(missense variant +1 more)
Short-rib thoracic dysplasia 13 with or without polydactyly
GPathogenic/Likely pathogenic