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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TBX2
(R20Q)
Single nucleotide variant
(missense variant)
TBX2-related disorder
+1 more
GPathogenic/Likely pathogenic
TBX2
(D116Y)
Single nucleotide variant
(missense variant)
Vertebral anomalies and variable endocrine and T-cell dysfunction
GUncertain significance
TBX2
(G144V)
Single nucleotide variant
(missense variant)
Vertebral anomalies and variable endocrine and T-cell dysfunction
GUncertain significance
TBX2
(K432R)
Single nucleotide variant
(missense variant)
Vertebral anomalies and variable endocrine and T-cell dysfunction
GUncertain significance
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