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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ABL1
(A397V +1 more)
Single nucleotide variant
(missense variant)
Congenital heart defects and skeletal malformations syndrome
GLikely pathogenic
ABL1
(R460S +1 more)
Single nucleotide variant
(missense variant)
Congenital heart defects and skeletal malformations syndrome
GUncertain significance
ABL1
(P784R +1 more)
Single nucleotide variant
(missense variant)
Congenital heart defects and skeletal malformations syndrome
GUncertain significance
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