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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
UNC80
(S1114T +2 more)
Single nucleotide variant
(missense variant)
Hypotonia, infantile, with psychomotor retardation and characteristic facies 2
+3 more
GConflicting classifications of pathogenicity
UNC80
(S1121R +2 more)
Single nucleotide variant
(missense variant)
See cases
GUncertain significance
UNC80
(R1886* +2 more)
Single nucleotide variant
(nonsense)
Hypotonia, infantile, with psychomotor retardation and characteristic facies 2
+2 more
GPathogenic
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