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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC114827851, MYH6
Single nucleotide variant
(synonymous variant)
not provided
+3 more
GBenign
LOC114827851, MYH6
Single nucleotide variant
(synonymous variant)
Cardiovascular phenotype
+3 more
GConflicting classifications of pathogenicity
LOC114827851, MYH6
(G56R)
Single nucleotide variant
(missense variant)
not provided
+3 more
GBenign
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