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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SCN5A
(Y1949C +5 more)
Single nucleotide variant
(missense variant)
Cardiac arrhythmia
+2 more
GUncertain significance
SCN5A
(R1846H +5 more)
Single nucleotide variant
(missense variant)
not provided
+4 more
GUncertain significance
SCN5A
(K1264N +2 more)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy
GUncertain significance
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