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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CHRNA2
(V349L +3 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
CHRNA2
(P161Q +2 more)
Single nucleotide variant
(missense variant +1 more)
Autosomal dominant nocturnal frontal lobe epilepsy
+1 more
GUncertain significance
CHRNA2
(T58I)
Single nucleotide variant
(missense variant +1 more)
Autosomal dominant nocturnal frontal lobe epilepsy 4
+3 more
GConflicting classifications of pathogenicity
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