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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
COL17A1
(D1200Y)
Single nucleotide variant
(missense variant)
Amelogenesis imperfecta
GPathogenic
COL17A1
(G567E)
Single nucleotide variant
(missense variant)
Amelogenesis imperfecta
GPathogenic