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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SPTAN1
(Q291fs +1 more)
Deletion
(frameshift variant)
not provided
GUncertain significance
SPTAN1
(K1466fs +2 more)
Deletion
(frameshift variant)
not provided
GUncertain significance
SPTAN1
(P1798fs +4 more)
Deletion
(frameshift variant)
Neurodevelopmental disorder
GLikely pathogenic
SPTAN1
(R2037W +4 more)
Single nucleotide variant
(missense variant)
Early infantile epileptic encephalopathy with suppression bursts
+3 more
GConflicting classifications of pathogenicity
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