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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RFC1
(R357* +1 more)
Single nucleotide variant
(nonsense)
Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome
GPathogenic/Likely pathogenic
RFC1
(N133S)
Single nucleotide variant
(missense variant)
Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome
GUncertain significance