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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130060335, LOC130060336
+242 more
Copy number gain
See cases
GPathogenic
MYOCD, MYOCD-AS1
Single nucleotide variant
(non-coding transcript variant +1 more)
not provided
GBenign