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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
VCL
(K815R)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 15
+4 more
GUncertain significance
MYH7
(S1836L)
Single nucleotide variant
(missense variant)
not specified
+8 more
GConflicting classifications of pathogenicity
MHRT, MYH7
(D1511V)
Single nucleotide variant
(non-coding transcript variant +1 more)
Hypertrophic cardiomyopathy
+1 more
GUncertain significance
MYH7
(E632del)
Deletion
Dilated cardiomyopathy 1S
GUncertain significance
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