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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
VLDLR
(R88Q)
Single nucleotide variant
(missense variant)
Cerebellar ataxia, intellectual disability, and dysequilibrium syndrome 1
GUncertain significance
VLDLR
(R257* +1 more)
Single nucleotide variant
(nonsense)
Cerebellar ataxia, intellectual disability, and dysequilibrium syndrome 1
GPathogenic
VLDLR
(R556Q +1 more)
Single nucleotide variant
(missense variant)
Cerebellar ataxia, intellectual disability, and dysequilibrium syndrome 1
+3 more
GUncertain significance
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