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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CRTAP
(S32G)
Single nucleotide variant
(missense variant)
Osteogenesis imperfecta type 7
+1 more
GUncertain significance
CRTAP
Deletion
(inframe_deletion)
Osteogenesis imperfecta type 7
+1 more
GUncertain significance
CRTAP
(L347F +2 more)
Single nucleotide variant
(missense variant)
Osteogenesis imperfecta type 7
+3 more
GConflicting classifications of pathogenicity
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