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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CHRNE
Single nucleotide variant
(splice donor variant)
Congenital myasthenic syndrome 4C
GPathogenic
C17orf107, CHRNE
(P141L)
Single nucleotide variant
(3 prime UTR variant +1 more)
not provided
+2 more
GPathogenic
C17orf107, CHRNE
(L98P)
Single nucleotide variant
(3 prime UTR variant +1 more)
Congenital myasthenic syndrome 4A
+2 more
GConflicting classifications of pathogenicity
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