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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KCTD7
(R181W)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
KCTD7
(D229Y)
Single nucleotide variant
(missense variant)
Progressive myoclonic epilepsy type 3
GLikely pathogenic