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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130059197, LOC130059198
+575 more
Copy number gain
See cases
GPathogenic
PRMT7, SLC7A6OS
(Q64R)
Single nucleotide variant
(missense variant)
Generalized myoclonic seizure
+1 more
GConflicting classifications of pathogenicity