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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
WNT10A
(R293C)
Single nucleotide variant
(missense variant)
Abnormality of the dentition
GUncertain significance
WNT10A
(R348C)
Single nucleotide variant
(missense variant)
Abnormality of the dentition
GUncertain significance