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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GAL
(A6T)
Single nucleotide variant
(missense variant)
Familial temporal lobe epilepsy 8
GUncertain significance
GAL
(D106H)
Single nucleotide variant
(missense variant)
Familial temporal lobe epilepsy 8
+1 more
GUncertain significance