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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
OR2T4
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
OR2T4
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
CNST, GCSAML
+58 more
Copy number loss
not provided
GPathogenic
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