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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TBX1
Deletion
(inframe_deletion)
DiGeorge syndrome
+3 more
GConflicting classifications of pathogenicity
TBX1
(A335V +1 more)
Single nucleotide variant
(missense variant)
DiGeorge syndrome
+3 more
GConflicting classifications of pathogenicity
TBX1
(P439T +1 more)
Single nucleotide variant
(missense variant +1 more)
Conotruncal heart malformations
+3 more
GConflicting classifications of pathogenicity
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