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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GREM2
(E136D)
Single nucleotide variant
(missense variant)
Tooth agenesis, selective, 9
GPathogenic
GREM2
(A13V)
Single nucleotide variant
(missense variant)
Tooth agenesis, selective, 9
GPathogenic