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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CRTAP
(H59fs)
Duplication
(frameshift variant)
Osteogenesis imperfecta type 7
GPathogenic
CRTAP
(R212* +1 more)
Single nucleotide variant
(nonsense)
Osteogenesis imperfecta type 7
GConflicting classifications of pathogenicity