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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NPR2
(G100S)
Single nucleotide variant
(missense variant)
Acromesomelic dysplasia 1, Maroteaux type
GLikely pathogenic
NPR2
(R165fs)
Deletion
(frameshift variant)
Acromesomelic dysplasia 1, Maroteaux type
GLikely pathogenic