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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CACNA1B
Single nucleotide variant
(synonymous variant)
Neurodevelopmental disorder with seizures and nonepileptic hyperkinetic movements
+2 more
GBenign
CACNA1B
(L2215R)
Single nucleotide variant
(synonymous variant +1 more)
Neurodevelopmental disorder with seizures and nonepileptic hyperkinetic movements
+2 more
GBenign
CACNA1B
Single nucleotide variant
(3 prime UTR variant)
Neurodevelopmental disorder with seizures and nonepileptic hyperkinetic movements
+2 more
GBenign
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