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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CHRNA4
(K439T +1 more)
Single nucleotide variant
(missense variant +1 more)
Autosomal dominant nocturnal frontal lobe epilepsy
+2 more
GConflicting classifications of pathogenicity
CHRNA4, LOC126863087
(E92Q)
Single nucleotide variant
(missense variant +2 more)
CHRNA4-related condition
+6 more
GConflicting classifications of pathogenicity