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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CHRNA4
Single nucleotide variant
(intron variant)
Autosomal dominant nocturnal frontal lobe epilepsy
+3 more
GBenign
CHRNA4
(R487Q +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
+5 more
GConflicting classifications of pathogenicity
CHRNA4
(N153S +1 more)
Single nucleotide variant
(missense variant +1 more)
Autosomal dominant nocturnal frontal lobe epilepsy
GUncertain significance
CHRNA4
Single nucleotide variant
(synonymous variant +2 more)
Autosomal dominant nocturnal frontal lobe epilepsy
+4 more
GBenign
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