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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TAB2
Deletion
(intron variant)
not provided
GUncertain significance
LOC126859827, TAB2
(S492fs +1 more)
Deletion
(frameshift variant)
Congenital heart defects, multiple types, 2
GPathogenic