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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FAM83H
Single nucleotide variant
(synonymous variant)
Amelogenesis imperfecta, hypocalcification type
+1 more
GBenign
FAM83H
Single nucleotide variant
(synonymous variant)
not specified
+2 more
GBenign