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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KCTD7
(T64A)
Single nucleotide variant
(missense variant)
not specified
+3 more
GConflicting classifications of pathogenicity
KCTD7
(R94W)
Single nucleotide variant
(missense variant)
Progressive myoclonic epilepsy type 3
GLikely pathogenic
KCTD7
(P161S)
Single nucleotide variant
(missense variant)
Progressive myoclonic epilepsy type 3
GUncertain significance
KCTD7
Deletion
(splice donor variant)
Progressive myoclonic epilepsy type 3
GLikely pathogenic
KCTD7
(R184C)
Single nucleotide variant
(missense variant)
not provided
+3 more
GPathogenic/Likely pathogenic
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