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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CHRNA2
(P226fs +3 more)
Deletion
(frameshift variant)
Autosomal dominant nocturnal frontal lobe epilepsy 4
+1 more
GUncertain significance
CHRNA2
(E171fs +3 more)
Deletion
(frameshift variant)
Autosomal dominant nocturnal frontal lobe epilepsy 4
GUncertain significance
CHRNA2
(R72P)
Single nucleotide variant
(missense variant +1 more)
not provided
+3 more
GConflicting classifications of pathogenicity
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