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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KCNC1
(R237W)
Single nucleotide variant
(missense variant)
Progressive myoclonic epilepsy type 7
GConflicting classifications of pathogenicity
KCNC1
(M262T)
Single nucleotide variant
(missense variant)
Progressive myoclonic epilepsy type 7
GUncertain significance
KCNC1
(V432M)
Single nucleotide variant
(missense variant)
not provided
+3 more
GConflicting classifications of pathogenicity
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