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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PLPBP
(P87L +3 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GPathogenic/Likely pathogenic
PLPBP
Single nucleotide variant
(splice acceptor variant)
Epilepsy, early-onset, vitamin B6-dependent
+1 more
GPathogenic
PLPBP
(D72fs +2 more)
Deletion
(frameshift variant)
not provided
+1 more
GPathogenic
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