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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SYN1
(I395T)
Single nucleotide variant
(missense variant)
Intellectual disability
GUncertain significance
SYN1
(Q249*)
Single nucleotide variant
(nonsense)
Intellectual disability, X-linked 50
+1 more
GPathogenic/Likely pathogenic
SYN1
(R114G)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
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