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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PLOD2
(T608I +1 more)
Single nucleotide variant
(missense variant)
Bruck syndrome 2
GPathogenic
PLOD2
(G601V +1 more)
Single nucleotide variant
(missense variant)
Bruck syndrome 2
GPathogenic
PLOD2
(R598H +1 more)
Single nucleotide variant
(missense variant)
Bruck syndrome 2
GConflicting classifications of pathogenicity
PLOD2
(V523fs)
Duplication
(frameshift variant +1 more)
not provided
GPathogenic
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