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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CAMTA1
(G832A +2 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
CAMTA1, LOC126805603
(S1258G +3 more)
Single nucleotide variant
(missense variant +1 more)
Cerebellar dysfunction with variable cognitive and behavioral abnormalities
GUncertain significance