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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ADRA2B
(R222*)
Single nucleotide variant
(nonsense)
not provided
+1 more
GConflicting classifications of pathogenicity
ADRA2B
(E217K)
Single nucleotide variant
(missense variant)
not specified
+1 more
GUncertain significance
ADRA2B
(D92N)
Single nucleotide variant
(missense variant)
Epilepsy, familial adult myoclonic, 2
GUncertain significance
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