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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SCN5A
(R1943* +5 more)
Single nucleotide variant
(nonsense)
not specified
+4 more
GConflicting classifications of pathogenicity
SCN5A
(A672T)
Single nucleotide variant
(missense variant)
not provided
+3 more
GConflicting classifications of pathogenicity
SCN5A
(R535Q)
Single nucleotide variant
(missense variant)
not specified
+5 more
GUncertain significance
SCN5A
(E446K)
Single nucleotide variant
(missense variant)
Brugada syndrome 1
+9 more
GConflicting classifications of pathogenicity
SCN5A
(E48K)
Single nucleotide variant
(missense variant)
Brugada syndrome 1
+5 more
GUncertain significance
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