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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SCN4B
(V203M +2 more)
Single nucleotide variant
(missense variant +1 more)
Long QT syndrome 10
+6 more
GConflicting classifications of pathogenicity
SCN4B
Single nucleotide variant
(synonymous variant +1 more)
SCN4B-related disorder
+2 more
GLikely benign
SCN4B
(G8S)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+3 more
GConflicting classifications of pathogenicity
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