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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CHRNA2
(W334* +3 more)
Single nucleotide variant
(nonsense)
Autosomal dominant nocturnal frontal lobe epilepsy 4
GUncertain significance
CHRNA2
(L41fs)
Deletion
(frameshift variant +1 more)
Autosomal dominant nocturnal frontal lobe epilepsy
+3 more
GUncertain significance