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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RELN, SLC26A5-AS1
(A3281fs)
Deletion
(frameshift variant)
Norman-Roberts syndrome
GLikely pathogenic
RELN
(F2105fs)
Deletion
(frameshift variant)
Familial temporal lobe epilepsy 7
GLikely pathogenic