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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RELN
(T1873I)
Single nucleotide variant
(missense variant)
not specified
+3 more
GConflicting classifications of pathogenicity
RELN
(S1719L)
Single nucleotide variant
(missense variant)
Norman-Roberts syndrome
+3 more
GConflicting classifications of pathogenicity