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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FGF12
(R114H +3 more)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 47
+2 more
GPathogenic
FGF12
(G112S +3 more)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 47
+1 more
GPathogenic/Likely pathogenic
FGF12
(T92A +2 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GConflicting classifications of pathogenicity
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