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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MYPN
(P87A)
Single nucleotide variant
(missense variant +2 more)
Dilated cardiomyopathy 1KK
+4 more
GUncertain significance
MYPN
(H324Y +1 more)
Single nucleotide variant
(missense variant +1 more)
Primary familial hypertrophic cardiomyopathy
GUncertain significance
MYPN
(T423M +1 more)
Single nucleotide variant
(missense variant +1 more)
Cardiovascular phenotype
+2 more
GUncertain significance
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