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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
WNT1
(L86fs)
Deletion
(frameshift variant)
Osteogenesis imperfecta type 15
GPathogenic
WNT1
(H111fs)
Duplication
(frameshift variant)
Osteogenesis imperfecta type 15
GLikely pathogenic