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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TBCK
Single nucleotide variant
(splice donor variant)
Hypotonia, infantile, with psychomotor retardation and characteristic facies 3
GLikely pathogenic
TBCK
(A116V)
Single nucleotide variant
(missense variant +2 more)
Hypotonia, infantile, with psychomotor retardation and characteristic facies 3
GUncertain significance