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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SPTBN2
(R2347Q +1 more)
Single nucleotide variant
(missense variant)
Spinocerebellar ataxia type 5
+1 more
GConflicting classifications of pathogenicity
SPTBN2
(V2246M)
Single nucleotide variant
(missense variant)
not specified
+2 more
GUncertain significance