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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CRTAP, LOC129936436
Single nucleotide variant
(synonymous variant)
Osteogenesis imperfecta type 7
+1 more
GConflicting classifications of pathogenicity
CRTAP, LOC129936436
(A8V)
Single nucleotide variant
(missense variant)
Osteogenesis imperfecta
+1 more
GUncertain significance
CRTAP, LOC129936436
Single nucleotide variant
(synonymous variant)
Osteogenesis imperfecta
GUncertain significance
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