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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MYH7
(Q1040R)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy
GUncertain significance
MYH7
(N696H)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1S
GLikely pathogenic
MYH7
(H666Q)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1S
GLikely pathogenic
MYH7
(R108H)
Single nucleotide variant
(missense variant)
Primary dilated cardiomyopathy
GUncertain significance
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