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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KCNC1
(A418S)
Single nucleotide variant
(missense variant)
Progressive myoclonic epilepsy type 7
+1 more
GUncertain significance
KCNC1
(E508D)
Single nucleotide variant
(missense variant)
Progressive myoclonic epilepsy type 7
+1 more
GUncertain significance
KCNC1
(P558R)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
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