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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SCN5A
Single nucleotide variant
(splice donor variant)
Long QT syndrome 3
+10 more
GPathogenic/Likely pathogenic
SCN5A
(Q646fs)
Deletion
(frameshift variant)
Brugada syndrome
+3 more
GPathogenic
SCN5A
Single nucleotide variant
(splice donor variant +1 more)
not provided
+1 more
GLikely pathogenic
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