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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SNX14
Single nucleotide variant
(splice donor variant +1 more)
not provided
GLikely pathogenic
SNX14
(E370* +12 more)
Single nucleotide variant
(nonsense +3 more)
Autosomal recessive spinocerebellar ataxia 20
+1 more
GPathogenic