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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DENND5A, DNHD1
+723 more
Copy number gain
See cases
GPathogenic
LOC130005303, SBF2
Microsatellite
(intron variant)
not provided
GBenign
LOC130005303, SBF2
Single nucleotide variant
(intron variant)
not provided
GBenign
SBF2, LOC130005303
Single nucleotide variant
(synonymous variant)
not specified
GLikely benign
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