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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ACCS, ACCSL
+225 more
Copy number loss
See cases
GPathogenic
EXT2, LOC130005598
Single nucleotide variant
(intron variant)
not specified
+2 more
GBenign
EXT2, LOC130005598
Single nucleotide variant
(intron variant)
not provided
GBenign
EXT2, LOC130005598
Single nucleotide variant
(intron variant)
not provided
GBenign
EXT2, LOC130005598
Single nucleotide variant
(intron variant)
not provided
GLikely benign
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