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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC126807556, SPARC
(E263K +1 more)
Single nucleotide variant
(missense variant)
Osteogenesis imperfecta type 17
GPathogenic
SPARC
(R166H +1 more)
Single nucleotide variant
(missense variant)
Osteogenesis imperfecta type 17
GPathogenic