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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PNKP
(Q517*)
Single nucleotide variant
(nonsense)
Inborn genetic diseases
+2 more
GConflicting classifications of pathogenicity
PNKP
(T424fs)
Duplication
(frameshift variant)
Intellectual disability
+5 more
GPathogenic
PNKP
Single nucleotide variant
(splice donor variant)
not provided
+6 more
GConflicting classifications of pathogenicity
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