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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ABL1
(T117M +1 more)
Single nucleotide variant
(missense variant)
Congenital heart defects and skeletal malformations syndrome
+1 more
GConflicting classifications of pathogenicity
ABL1
(V506M +1 more)
Single nucleotide variant
(missense variant)
Congenital heart defects and skeletal malformations syndrome
GPathogenic
ABL1
(G511R +1 more)
Single nucleotide variant
(missense variant)
Congenital heart defects and skeletal malformations syndrome
GUncertain significance
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