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Items: 7

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MYL3
Single nucleotide variant
(intron variant)
not specified
+1 more
GBenign/Likely benign
MYL3
Single nucleotide variant
(intron variant)
not provided
GLikely benign
MYL3
(D141N)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy
+1 more
GUncertain significance
MYL3
Single nucleotide variant
(intron variant)
not provided
+3 more
GConflicting classifications of pathogenicity
MYL3
(G74R)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 8
+4 more
GConflicting classifications of pathogenicity
MYL3
(R63C)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+3 more
GUncertain significance
MYL3
Single nucleotide variant
(intron variant)
not specified
+4 more
GBenign/Likely benign
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