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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
VCL
(H184Y)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 15
+3 more
GUncertain significance
VCL
(T643M)
Single nucleotide variant
(missense variant)
not provided
+3 more
GUncertain significance
VCL
(V1127I +1 more)
Single nucleotide variant
(missense variant)
Wolff-Parkinson-White pattern
GUncertain significance
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