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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SCN4A, GH-LCR
(I1455T)
Single nucleotide variant
(missense variant)
Congenital myasthenic syndrome 16
+6 more
GConflicting classifications of pathogenicity
GH-LCR, SCN4A
(T1313M)
Single nucleotide variant
(missense variant)
Hyperkalemic periodic paralysis
+7 more
GPathogenic