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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RELN, SLC26A5-AS1
(M3434V +1 more)
Single nucleotide variant
(missense variant)
Intellectual disability
+2 more
GUncertain significance
RELN
(E1356A)
Single nucleotide variant
(missense variant)
Seizure
GUncertain significance
RELN
(P672L)
Single nucleotide variant
(missense variant)
Norman-Roberts syndrome
+3 more
GConflicting classifications of pathogenicity
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