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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
COLQ
Single nucleotide variant
(splice donor variant)
Congenital myasthenic syndrome 5
GPathogenic
COLQ
(P263L +2 more)
Single nucleotide variant
(missense variant)
Congenital myasthenic syndrome 5
+2 more
GUncertain significance