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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SYNE1
(R5300* +1 more)
Single nucleotide variant
(nonsense)
Autosomal recessive ataxia, Beauce type
+1 more
GPathogenic
SYNE1
(R5254* +1 more)
Single nucleotide variant
(nonsense)
Autosomal recessive ataxia, Beauce type
+2 more
GPathogenic
SYNE1
(E1721* +1 more)
Single nucleotide variant
(nonsense)
Autosomal recessive ataxia, Beauce type
+1 more
GPathogenic
SYNE1
(F33fs)
Deletion
(frameshift variant)
Autosomal recessive ataxia, Beauce type
GPathogenic
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