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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CYP26B1
(M318I +1 more)
Single nucleotide variant
(missense variant)
Craniosynostosis syndrome
GUncertain significance
CYP26B1
(V28fs)
Duplication
(frameshift variant)
Craniosynostosis syndrome
GUncertain significance