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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MYL3
(V156L)
Single nucleotide variant
(missense variant)
not specified
+5 more
GConflicting classifications of pathogenicity
MYL3
(R154H)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+4 more
GUncertain significance
MYL3
(A57G)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+5 more
GConflicting classifications of pathogenicity
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