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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RFC1
Single nucleotide variant
(stop lost)
not provided
GUncertain significance
ABLIM2, ACOX3
+226 more
Copy number gain
See cases
GPathogenic
CHRNA9, CWH43
+54 more
Copy number gain
See cases
GPathogenic
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