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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SCN5A
(E1822K +5 more)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1E
+10 more
GUncertain significance
SCN5A
(D1736N +5 more)
Single nucleotide variant
(missense variant)
Progressive familial heart block, type 1A
+8 more
GUncertain significance