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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC108663996, TBP
(Q95del +1 more)
Deletion
(inframe_deletion)
Spinocerebellar ataxia type 17
+1 more
GBenign
LOC108663996, TBP
Single nucleotide variant
(synonymous variant)
not provided
+3 more
GBenign/Likely benign