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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SCN5A
(D2002N +5 more)
Single nucleotide variant
(missense variant)
not specified
+11 more
GUncertain significance
SCN5A
(G1390R +2 more)
Single nucleotide variant
(missense variant)
not provided
+10 more
GUncertain significance
SCN5A
(T1303M +2 more)
Single nucleotide variant
(missense variant)
Conduction disorder of the heart
+6 more
GUncertain significance
SCN5A
(Q692K)
Single nucleotide variant
(missense variant)
Long QT syndrome
+11 more
GConflicting classifications of pathogenicity
SCN5A
(A447G)
Single nucleotide variant
(missense variant)
not specified
+11 more
GConflicting classifications of pathogenicity
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