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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ARFGEF1-DT, CPA6
(Y336C)
Single nucleotide variant
(missense variant)
Familial temporal lobe epilepsy 5
GUncertain significance
CPA6
(W148R)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance