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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SCYL1
(R151*)
Single nucleotide variant
(nonsense)
Acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome
GPathogenic
SCYL1
(M268I)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
SCYL1
(G739A +1 more)
Single nucleotide variant
(missense variant)
Acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome
GUncertain significance
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