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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TBX3
(A488T +1 more)
Single nucleotide variant
(missense variant)
Ulnar-mammary syndrome
GUncertain significance
TBX3
(E360D +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
TBX3
(I234V +1 more)
Single nucleotide variant
(missense variant)
Ulnar-mammary syndrome
GConflicting classifications of pathogenicity
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