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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RUNX2
(M161V +1 more)
Single nucleotide variant
(missense variant)
Cleidocranial dysostosis
+1 more
GConflicting classifications of pathogenicity
RUNX2
(P288L +1 more)
Single nucleotide variant
(missense variant)
Metaphyseal dysplasia-maxillary hypoplasia-brachydacty syndrome
+1 more
GUncertain significance
RUNX2
Single nucleotide variant
(splice donor variant)
Cleidocranial dysostosis
GLikely pathogenic
ERVH-3, ETV7
+427 more
Copy number gain
not provided
GPathogenic
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