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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TTBK2
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
TTBK2
(L8P)
Single nucleotide variant
(missense variant)
not specified
+2 more
GBenign
TTBK2
Single nucleotide variant
(5 prime UTR variant)
Spinocerebellar ataxia type 11
+3 more
GBenign
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