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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KCTD7
(R153H)
Single nucleotide variant
(missense variant)
Progressive myoclonic epilepsy type 3
+1 more
GLikely pathogenic; Affects
KCTD7
(Q255E)
Single nucleotide variant
(missense variant)
Progressive myoclonic epilepsy type 3
GUncertain significance