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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SNX14
(R816Q +16 more)
Single nucleotide variant
(missense variant +2 more)
Autosomal recessive spinocerebellar ataxia 20
GUncertain significance
SNX14
(R111* +4 more)
Single nucleotide variant
(nonsense +2 more)
Autosomal recessive spinocerebellar ataxia 20
GPathogenic