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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SCN5A
(L1732fs +5 more)
Deletion
(frameshift variant)
Cardiac arrhythmia
+2 more
GPathogenic/Likely pathogenic
SCN5A
(F1616del +5 more)
Microsatellite
(inframe_deletion)
Cardiovascular phenotype
+11 more
GPathogenic/Likely pathogenic
SCN5A
Microsatellite
(intron variant)
Brugada syndrome 1
+1 more
GLikely pathogenic
SCN5A
(R1512W +4 more)
Single nucleotide variant
(missense variant)
Cardiac arrhythmia
+3 more
GConflicting classifications of pathogenicity
SCN5A
(R282C)
Single nucleotide variant
(missense variant)
not specified
+2 more
GConflicting classifications of pathogenicity
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