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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TRDN
(P712L)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
TRDN
(L470M)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+2 more
GBenign/Likely benign
TRDN
Single nucleotide variant
(intron variant)
not specified
+2 more
GBenign
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