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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MYPN
(S312F +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+2 more
GConflicting classifications of pathogenicity
MYPN
(S1056F +1 more)
Single nucleotide variant
(missense variant +1 more)
Hypertrophic cardiomyopathy
+2 more
GLikely benign
MYPN
(R1091W +1 more)
Single nucleotide variant
(missense variant +1 more)
Cardiovascular phenotype
+3 more
GUncertain significance
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