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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130065679, SNTA1
(G96A)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+4 more
GConflicting classifications of pathogenicity
SNTA1
(A67V)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+2 more
GUncertain significance