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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC132089226, LOC132089227
+1167 more
Copy number gain
See cases
GPathogenic
BOD1
(R112*)
Single nucleotide variant
(nonsense +1 more)
not provided
GPathogenic
BOD1
Single nucleotide variant
(intron variant)
not provided
GUncertain significance
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