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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ABLIM3, ACSL6
+1672 more
Copy number loss
See cases
GPathogenic
LOC132089226, LOC132089227
+1167 more
Copy number gain
See cases
GPathogenic
LOC129995011, SYNPO
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GBenign/Likely benign
LOC129995011, SYNPO
Microsatellite
(inframe_deletion)
not provided
GConflicting classifications of pathogenicity
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