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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SNTA1
(A257G)
Single nucleotide variant
(missense variant)
not specified
+6 more
GConflicting classifications of pathogenicity
SNTA1
(P74L)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+5 more
GConflicting classifications of pathogenicity
SNTA1
(P56S)
Single nucleotide variant
(missense variant)
Long QT syndrome
+3 more
GBenign
LOC130065680, SNTA1
Single nucleotide variant
(5 prime UTR variant)
Long QT syndrome 1
GUncertain significance
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