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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KCTD7
Single nucleotide variant
(synonymous variant)
Progressive myoclonic epilepsy type 3
+3 more
GBenign
KCTD7
Duplication
(intron variant)
not specified
+2 more
GBenign