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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SCN5A
(T1930I +5 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
SCN5A
(V1352M +2 more)
Single nucleotide variant
(missense variant)
Sick sinus syndrome 1
+7 more
GConflicting classifications of pathogenicity
SCN5A
(S571I)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+2 more
GUncertain significance
SCN5A
Single nucleotide variant
(splice donor variant)
Brugada syndrome
+4 more
GPathogenic
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