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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TPM1
(A22T)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+5 more
GConflicting classifications of pathogenicity
TPM1
(K29Q)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 3
GUncertain significance
TPM1
(I171M +2 more)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 3
+1 more
GUncertain significance
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