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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
EDA
(S160R)
Single nucleotide variant
(missense variant)
Tooth agenesis, selective, X-linked, 1
GUncertain significance
EDA
(R357W +2 more)
Single nucleotide variant
(missense variant)
See cases
+2 more
GPathogenic/Likely pathogenic