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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DSPP
(V18D)
Single nucleotide variant
(missense variant)
Dentinogenesis imperfecta type 2
GLikely pathogenic
DSPP
(N1232fs)
Deletion
(frameshift variant)
Dentinogenesis imperfecta type 2
GUncertain significance