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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
COMP
(N523K)
Single nucleotide variant
(missense variant)
not provided
+1 more
GPathogenic/Likely pathogenic
COMP
(D439N)
Single nucleotide variant
(missense variant)
Multiple epiphyseal dysplasia type 1
GLikely pathogenic
COMP
(P296R)
Single nucleotide variant
(missense variant)
Multiple epiphyseal dysplasia type 1
GLikely pathogenic
COMP
(C255R)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
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