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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SCN5A
(V1596M +4 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+9 more
GUncertain significance
LOC110121269, SCN5A
(A993V)
Single nucleotide variant
(missense variant +1 more)
Long QT syndrome 3
GUncertain significance
SCN5A
(Q692K)
Single nucleotide variant
(missense variant)
Long QT syndrome
+11 more
GConflicting classifications of pathogenicity
SCN5A
(S216L)
Single nucleotide variant
(missense variant +1 more)
Ventricular fibrillation, paroxysmal familial, type 1
+13 more
GConflicting classifications of pathogenicity
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