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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SCN5A
(S1913fs +5 more)
Deletion
(frameshift variant +1 more)
Brugada syndrome 1
GUncertain significance
SCN5A
(E1784K +5 more)
Single nucleotide variant
(missense variant)
not provided
+7 more
GPathogenic/Likely pathogenic
SCN5A
(K1492del +4 more)
Microsatellite
(inframe_deletion)
Brugada syndrome
+2 more
GPathogenic/Likely pathogenic
SCN5A
(N1215S +2 more)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+8 more
GUncertain significance
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