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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SHANK3
(S1026F +1 more)
Single nucleotide variant
(missense variant)
Atypical behavior
+4 more
GUncertain significance
SHANK3
(P1329S)
Single nucleotide variant
(missense variant)
Phelan-McDermid syndrome
+1 more
GConflicting classifications of pathogenicity
SHANK3
(P1384S)
Single nucleotide variant
(missense variant)
Phelan-McDermid syndrome
GUncertain significance
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