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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MYO9A
(G2282E)
Single nucleotide variant
(missense variant)
Myasthenic syndrome, congenital, 24, presynaptic
+1 more
GConflicting classifications of pathogenicity
MYO9A
(Y203C)
Single nucleotide variant
(missense variant)
Myasthenic syndrome, congenital, 24, presynaptic
+1 more
GUncertain significance