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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CNOT3, LENG1
Single nucleotide variant
(3 prime UTR variant +1 more)
CNOT3-related disorder
GUncertain significance
CNOT3, LENG1
Single nucleotide variant
(3 prime UTR variant)
CNOT3-related disorder
GLikely benign