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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TFAP2B
(A275D)
Single nucleotide variant
(missense variant)
Char syndrome
GPathogenic
TFAP2B
(T306M)
Single nucleotide variant
(missense variant)
Char syndrome
GUncertain significance
TFAP2B
(D369H)
Single nucleotide variant
(missense variant)
Char syndrome
GUncertain significance
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