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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TWNK
(L17fs)
Deletion
(non-coding transcript variant +2 more)
Infantile onset spinocerebellar ataxia
GPathogenic
TWNK
(R400L)
Single nucleotide variant
(missense variant +2 more)
Infantile onset spinocerebellar ataxia
GLikely pathogenic
TWNK
(N438K)
Single nucleotide variant
(missense variant +2 more)
Infantile onset spinocerebellar ataxia
GLikely pathogenic
TWNK
(R543Q +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GConflicting classifications of pathogenicity
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