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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TCAP
(R17C)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+4 more
GUncertain significance
TCAP
(P141A)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+3 more
GUncertain significance
TCAP
(G150S)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+6 more
GUncertain significance
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