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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MYPN
(D369N +1 more)
Single nucleotide variant
(missense variant +1 more)
Hypertrophic cardiomyopathy
+3 more
GUncertain significance
MYPN
Single nucleotide variant
(splice acceptor variant)
Dilated cardiomyopathy 1KK
GLikely pathogenic