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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ARFGEF1-DT, CPA6
(V364L)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ARFGEF1-DT, CPA6
(V364I)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
ARFGEF1-DT, CPA6
(H313Q)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
CPA6
(H156Y)
Single nucleotide variant
(missense variant)
Familial temporal lobe epilepsy 5
+1 more
GUncertain significance
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