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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CDT1
(A66T)
Single nucleotide variant
(missense variant)
Meier-Gorlin syndrome 4
GPathogenic
CDT1
(Q117H)
Single nucleotide variant
(missense variant)
Meier-Gorlin syndrome 4
GPathogenic
CDT1
(R462Q)
Single nucleotide variant
(missense variant)
Meier-Gorlin syndrome
+1 more
GPathogenic/Likely pathogenic
CDT1
(E468K)
Single nucleotide variant
(missense variant)
not provided
GLikely pathogenic
CDT1
(Y520*)
Single nucleotide variant
(nonsense)
Meier-Gorlin syndrome 4
GPathogenic
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