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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FGF12
(P110S +3 more)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 47
GUncertain significance
FGF12
(D102H +2 more)
Single nucleotide variant
(missense variant +1 more)
Developmental and epileptic encephalopathy, 47
GUncertain significance
FGF12
(E42K)
Single nucleotide variant
(missense variant +1 more)
Developmental and epileptic encephalopathy, 47
+1 more
GUncertain significance
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