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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ELOVL5
(V190A)
Single nucleotide variant
(synonymous variant +1 more)
Spinocerebellar ataxia type 38
GUncertain significance
ELOVL5
(R111H +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance