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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LAMB3
(R1164C)
Single nucleotide variant
(missense variant)
Amelogenesis imperfecta type 1A
GUncertain significance
LAMB3
(G1102fs)
Deletion
(frameshift variant)
Amelogenesis imperfecta type 1A
GLikely pathogenic
LAMB3
(V976fs)
Deletion
(frameshift variant)
Amelogenesis imperfecta type 1A
GLikely pathogenic
LAMB3
Single nucleotide variant
(intron variant)
Amelogenesis imperfecta type 1A
GUncertain significance
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