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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FHOD3
(S635R +2 more)
Single nucleotide variant
(missense variant)
Cardiomyopathy, familial hypertrophic, 28
GUncertain significance
C18orf21, CELF4
+7 more
Copy number loss
not provided
GPathogenic