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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SPEN
(R31H)
Single nucleotide variant
(missense variant)
Developmental disorder
+1 more
GConflicting classifications of pathogenicity
SPEN
(E1449*)
Single nucleotide variant
(nonsense)
Radio-Tartaglia syndrome
GPathogenic