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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MYH6
(T1379M)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+4 more
GConflicting classifications of pathogenicity
MYH6
(Q1065H)
Single nucleotide variant
(missense variant)
Migraine
+7 more
GConflicting classifications of pathogenicity
MYH6
(D588A)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 14
+5 more
GConflicting classifications of pathogenicity
MYH6
(I275N)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+6 more
GConflicting classifications of pathogenicity
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