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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SNTA1
(A257G)
Single nucleotide variant
(missense variant)
Long QT syndrome 12
+6 more
GConflicting classifications of pathogenicity
SNTA1
(R106Q)
Single nucleotide variant
(missense variant)
Primary dilated cardiomyopathy
+5 more
GBenign/Likely benign
LOC130065680, SNTA1
Single nucleotide variant
(synonymous variant)
not specified
+3 more
GBenign/Likely benign
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